Allele Registry

Canonical Allele Identifier: PA2825920688

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV003555147

ClinVar Variation:

2734649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Gly831Ala	CA320333 NM_001145853.1:c.2492G>C