Canonical Allele Identifier: PA645508181
Gene: XDH HGNC NCBI

Linked Data

ClinVar Variation Id: 335788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000370.2:p.Ser425Cys
CA1599278
NM_000379.4:c.1274C>G