Canonical Allele Identifier: PA2825919959
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1698065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala406Thr
CA91796236
NM_001145853.1:c.1216G>A