Canonical Allele Identifier: PA105526
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 198835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg558Cys
CA275434
NM_001145853.1:c.1672C>T