Canonical Allele Identifier: PA2825920414
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Gly674Arg
CA321852
NM_001145853.1:c.2020G>A
CA2839574
NM_001145853.1:c.2020G>C