Canonical Allele Identifier: PA179672
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166604
ClinVar RCV Id: RCV000152693 RCV003128187
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Cys765Arg
CA179671
NM_006005.3:c.2293T>C