Allele Registry

Canonical Allele Identifier: PA321655

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000197209

RCV002467661

RCV004541270

ClinVar Variation:

215397

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg732His	CA321654 NM_006005.3:c.2195G>A