Canonical Allele Identifier: PA2825920105
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val493Ala
CA2839367
NM_001145853.1:c.1478T>C