Allele Registry

Canonical Allele Identifier: PA658812762

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000730495

ClinVar Variation:

516852

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Ala58Val	CA2838811 NM_006005.3:c.173C>T