Allele Registry

Canonical Allele Identifier: PA2825920623

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000218719

RCV001393083

ClinVar Variation:

229641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Ser790Leu	CA2839705 NM_001145853.1:c.2369C>T