Canonical Allele Identifier: PA2825919686
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2061925
ClinVar RCV Id: RCV002953047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Ser222Tyr
CA356172263
NM_001145853.1:c.665C>A