Allele Registry

Canonical Allele Identifier: PA319809

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000195462

RCV002509047

RCV002517273

ClinVar Variation:

215355

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Asp379Asn	CA319808 NM_006005.3:c.1135G>A