Allele Registry

Canonical Allele Identifier: PA2825920497

Gene: WFS1 HGNC NCBI

ClinVar Allele:

443628

ClinVar RCV:

RCV000518926

RCV002490902

ClinVar Variation:

449390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Glu717Lys	CA2839622 NM_001145853.1:c.2149G>A