Allele Registry

Canonical Allele Identifier: PA2825920356

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV003087715

ClinVar Variation:

2160759

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Lys634Arg	CA2839539 NM_001145853.1:c.1901A>G