Allele Registry

Canonical Allele Identifier: PA2825920438

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV001196420

RCV001863106

ClinVar Variation:

930623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Ala684Gly	CA356177610 NM_001145853.1:c.2051C>G