Allele Registry

Canonical Allele Identifier: PA105651

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000023518

RCV001762055

ClinVar Variation:

30559

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Gly780Ser	CA129330 NM_001145853.1:c.2338G>A