Canonical Allele Identifier: PA101463
Gene: UROD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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