Home
Career Stage
Medical Students Residents Attendings CPT Codes Resources Blog Support

81303 Mecp2 gene known variant

Pathology & Lab

Also known as: MECP2 familial variant testing, Rett syndrome family screening

Methyl-CpG-binding protein 2 (MECP2) gene analysis for known familial variants to facilitate screening in Rett syndrome families.

Clinical Context

Targeted MECP2 testing of at-risk family members for previously identified variants in Rett syndrome families.

RVU Breakdown

Work RVU0.00
Practice Expense RVU0.00
Malpractice RVU0.00
Total RVU0.00

Specialties

PathologyNeurologyGenetics

Track This Code in RVU Edge

Log procedures, calculate wRVUs, and benchmark against MGMA data — all in one app.

CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.