Canonical Allele Identifier: PA2825920349
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Arg629Gln
CA261748
NM_001145853.1:c.1886G>A