Allele Registry

Canonical Allele Identifier: PA179674

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000152694

RCV003147359

ClinVar Variation:

166605

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Phe775Val	CA179673 NM_006005.3:c.2323T>G