Allele Registry

Canonical Allele Identifier: PA179676

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000152695

RCV000351538

RCV000658991

RCV000664094

RCV001157779

RCV001544546

RCV004532715

ClinVar Variation:

166606

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Glu776Val	CA179675 NM_006005.3:c.2327A>T