Allele Registry

Canonical Allele Identifier: PA916010553

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000998218

ClinVar Variation:

809619

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Arg859Leu	CA356179283 NM_006005.3:c.2576G>T