Canonical Allele Identifier: PA2825920191
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2002106
ClinVar RCV Id: RCV002832905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Cys541Gly
CA356176310
NM_001145853.1:c.1621T>G