Canonical Allele Identifier: PA2825920295
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala598Thr
CA182628
NM_001145853.1:c.1792G>A