Canonical Allele Identifier: PA2825920135
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Tyr508Cys
CA356175816
NM_001145853.1:c.1523A>G