Canonical Allele Identifier: PA645508189
Gene: XDH HGNC NCBI

Linked Data

ClinVar Variation Id: 335769
ClinVar RCV Id: RCV000370785 RCV001485627 RCV003932333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000370.2:p.Gly951Arg
CA1598647
NM_000379.4:c.2851G>A
CA346500274
NM_000379.4:c.2851G>C