Allele Registry

Canonical Allele Identifier: PA320895

Gene: WFS1 HGNC NCBI

ClinVar Allele:

211035

ClinVar RCV:

RCV000196477

RCV004020438

ClinVar Variation:

215378

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Asp211Asn	CA320894 NM_006005.3:c.631G>A