Canonical Allele Identifier: PA2825920465
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg703Cys
CA2839602
NM_001145853.1:c.2107C>T