Allele Registry

Canonical Allele Identifier: PA1139700111

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV001198917

RCV002491598

ClinVar Variation:

931915

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg868Pro	CA91797871 NM_006005.3:c.2603G>C