Last updated: October 2026CMS rates · Free lookup
Medicare Fee Schedule Lookup
Search 2026 Medicare reimbursement rates and national payment amounts by CPT, HCPCS, MS-DRG, or NDC code. The lookup includes the Physician Fee Schedule, Drug ASP, MS-DRG weights and national rates, anesthesia conversion factors, the Clinical Laboratory Fee Schedule, DMEPOS, ambulance, opioid treatment program, and Part D negotiated price data from CMS.
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81401
20262025
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Related codes
81400Mopath Procedure Level 1, Molecular Pathology Procedure Level 1 (Eg Identification Of Single Germline Variant [Eg Snp] By Techniques Such As Restriction Enzyme Digestion Or Melt Curve Analysis) Acadm (Acyl-Coa Dehydrogenase C-4 To C-12 Straight Chain Mcad) (Eg Medium Chain Acyl Dehydrogenase Deficiency) K304e Variant Ace (Angiotensin Converting Enzyme) (Eg Hereditary Blood Pressure Regulation) Insertion Deletion Variant Agtr1 (Angiotensin Ii Receptor Type 1) (Eg Essential Hypertension) 1166a>C Variant Bckdha (Branched Chain Keto Acid Dehydrogenase E1 Alpha Polypeptide) (Eg Maple Syrup Urine Disease Type 1a) Y438n Variant Ccr5 (Chemokine C-C Motif Receptor 5) (Eg Hiv Resistance) 32-Bp Deletion Mutation 794 825del32 Deletion Clrn1 (Clarin 1) (Eg Usher Syndrome Type 3) N48k Variant F2 (Coagulation Factor 2) (Eg Hereditary Hypercoagulability) 1199g>A Variant F5 (Coagulation Factor V) (Eg Hereditary Hypercoagulability) Hr2 Variant F7 (Coagulation Factor Vii [Serum Prothrombin Conversion Accelerator]) (Eg Hereditary Hypercoagulability) R353q Variant F13b (Coagulation Factor Xiii B Polypeptide) (Eg Hereditary Hypercoagulability) V34l Variant Fgb (Fibrinogen Beta Chain) (Eg Hereditary Ischemic Heart Disease) -455g>A Variant Fgfr1 (Fibroblast Growth Factor Receptor 1) (Eg Pfeiffer Syndrome Type 1 Craniosynostosis) P252r Variant Fgfr3 (Fibroblast Growth Factor Receptor 3) (Eg Muenke Syndrome) P250r Variant Fktn (Fukutin) (Eg Fukuyama Congenital Muscular Dystrophy) Retrotransposon Insertion Variant Gne (Glucosamine [Udp-N-Acetyl]-2-Epimerase N-Acetylmannosamine Kinase) (Eg Inclusion Body Myopathy 2 [Ibm2] Nonaka Myopathy) M712t Variant Ivd (Isovaleryl-Coa Dehydrogenase) (Eg Isovaleric Acidemia) A282v Variant Lct (Lactase-Phlorizin Hydrolase) (Eg Lactose Intolerance) 13910 C>T Variant Neb (Nebulin) (Eg Nemaline Myopathy 2) Exon 55 Deletion Variant Pcdh15 (Protocadherin-Related 15) (Eg Usher Syndrome Type 1f) R245x Variant Serpine1 (Serpine Peptidase Inhibitor Clade E Member 1 Plasminogen Activator Inhibitor -1 Pai-1) (Eg Thrombophilia) 4g Variant Shoc2 (Soc-2 Suppressor Of Clear Homolog) (Eg Noonan-Like Syndrome With Loose Anagen Hair) S2g Variant Sry (Sex Determining Region Y) (Eg 46xx Testicular Disorder Of Sex Development Gonadal Dysgenesis) Gene Analysis Tor1a (Torsin Family 1 Member A [Torsin A]) (Eg Early-Onset Primary Dystonia [Dyt1]) 907 909delgag (904 906delgag) Variant
$63.9681402Mopath Procedure Level 3, Molecular Pathology Procedure Level 3 Eg 10 Snps 2 10 Methylated Variants Or 2 10 Somatic Variants Typically Using Non Sequencing Target Variant Analysis Immunoglobulin And T Cell Receptor Gene Rearrangements Duplication Deletion Variants Of 1 Exon Loss Of Heterozygosity Loh Uniparental Disomy Upd Chromosome 1p 19q Eg Glial Tumors Deletion Analysis Chromosome 18q Eg D18s55 D18s58 D18s61 D18s64 And D18s69 Eg Colon Cancer Allelic Imbalance Assessment Ie Loss Of Heterozygosity Col1a1 Pdgfb T 17 22 Eg Dermatofibrosarcoma Protuberans Translocation Analysis Multiple Breakpoints Qualitative And Quantitative If Performed Cyp21a2 Cytochrome P450 Family 21 Subfamily A Polypeptide 2 Eg Congenital Adrenal Hyperplasia 21 Hydroxylase Deficiency Common Variants Eg Ivs2 13g P30l I172n Exon 6 Mutation Cluster I235n V236e M238k V281l L307ffsx6 Q318x R356w P453s G110vfsx21 30 Kb Deletion Variant Esr1 Pgr Receptor 1 Progesterone Receptor Ratio Eg Breast Cancer Mefv Mediterranean Fever Eg Familial Mediterranean Fever Common Variants Eg E148q P369s F479l M680i I692del M694v M694i K695r V726a A744s R761h Trd T Cell Antigen Receptor Delta Eg Leukemia And Lymphoma Gene Rearrangement Analysis Evaluation To Detect Abnormal Clonal Population Uniparental Disomy Upd Eg Russell Silver Syndrome Prader Willi Angelman Syndrome Short Tandem Repeat Str Analysis
$150.33Methodology
Rates come from the CMS Clinical Laboratory Fee Schedule (CLFS), published quarterly. Each HCPCS payment amount reflects the national CLFS payment for outpatient laboratory services.
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