Allele Registry

Canonical Allele Identifier: PA2825919660

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000486801

RCV002469171

ClinVar Variation:

420050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Glu202Gly	CA16618051 NM_001145853.1:c.605A>G