Allele Registry

Canonical Allele Identifier: PA261749

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038647

RCV000196272

RCV001174425

RCV002513507

RCV003125863

ClinVar Variation:

45443

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg629Gln	CA261748 NM_006005.3:c.1886G>A