Allele Registry

Canonical Allele Identifier: PA236438

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000171514

RCV001303065

RCV002498858

ClinVar Variation:

191322

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Val288Met	CA236437 NM_006005.3:c.862G>A