Allele Registry

Canonical Allele Identifier: PA320080

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV001705136

RCV002478695

RCV003126588

ClinVar Variation:

215372

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Pro19Leu	CA320079 NM_006005.3:c.56C>T