Canonical Allele Identifier: PA101463
Gene: UROD HGNC NCBI

Linked Data

ClinVar Variation Id: 69
ClinVar RCV Id: RCV000000087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000365.3:p.Arg292Gly
CA251373
NM_000374.5:c.874C>G