Canonical Allele Identifier: PA2825920521
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Met731Val
CA2839640
NM_001145853.1:c.2191A>G