Canonical Allele Identifier: PA105509
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ala716Thr
CA253197
NM_001145853.1:c.2146G>A