Allele Registry

Canonical Allele Identifier: PA320197

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000727080

RCV002500615

RCV002509294

RCV004530179

ClinVar Variation:

215386

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Trp399Gly	CA320196 NM_006005.3:c.1195T>G