Allele Registry

Canonical Allele Identifier: PA261753

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000038651

ClinVar Variation:

45447

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Asn714Thr	CA261752 NM_006005.3:c.2141A>C