Allele Registry

Canonical Allele Identifier: PA101496

Gene: UROD HGNC NCBI

ClinVar RCV:

RCV000000086

RCV001804706

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_000365.3:p.Glu167Lys	CA251372 NM_000374.5:c.499G>A