Canonical Allele Identifier: PA645508178
Gene: XDH HGNC NCBI

Linked Data

ClinVar Variation Id: 335796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000370.2:p.Pro206Leu
CA1599557
NM_000379.4:c.617C>T