Allele Registry

Canonical Allele Identifier: PA2825920738

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000998218

ClinVar Variation:

809619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139325.1:p.Arg859Leu	CA356179283 NM_001145853.1:c.2576G>T