Allele Registry

Canonical Allele Identifier: PA2825919382

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000152662

RCV002509039

ClinVar Variation:

166568

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Ala43Val	CA179627 NM_001145853.1:c.128C>T