Allele Registry

Canonical Allele Identifier: PA261751

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038650

ClinVar Variation:

45446

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg685Pro	CA261750 NM_006005.3:c.2054G>C