Allele Registry

Canonical Allele Identifier: PA101565

Gene: UROD HGNC NCBI

ClinVar RCV:

RCV000000082

RCV002512589

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_000365.3:p.Gly281Val	CA251370 NM_000374.5:c.842G>T