Canonical Allele Identifier: PA2825920442
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg685Cys
CA2839583
NM_001145853.1:c.2053C>T