Variants
Sign InSign Up

rs730880029

  • Pathogenic

Your Genotype

Sign In

Description

Reference Allele

T


Alternative Allele

G

Chromosome

2


Location

219251266


Variant Type

SNP

Genes

ClinVar

Name

NM_006000.3(TUBA4A):c.433A>C (p.Thr145Pro)


Allele

G


Clinical Significance

Pathogenic

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.