Allele Registry

Canonical Allele Identifier: PA645503102

Gene: UROD HGNC NCBI

ClinVar RCV:

RCV000493784

ClinVar Variation:

430039

HGVS (amino-acid)	Matching Registered Transcripts
NP_000365.3:p.Arg292Trp	CA825359 NM_000374.5:c.874C>T