Canonical Allele Identifier: PA2499272359
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Tyr508Cys
CA356175816
NM_006005.3:c.1523A>G