Canonical Allele Identifier: PA322819
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215392
ClinVar RCV Id: RCV000198315 RCV003126589
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Gly562Arg
CA322818
NM_006005.3:c.1684G>C