Allele Registry

Canonical Allele Identifier: PA105587

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000196664

RCV004530178

ClinVar Variation:

215376

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Glu169Lys	CA321089 NM_001145853.1:c.505G>A