Canonical Allele Identifier: PA2825920245
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 504710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala569Val
CA2839455
NM_001145853.1:c.1706C>T