Allele Registry

Canonical Allele Identifier: PA122089

Gene: UGT1A3 HGNC NCBI

ClinVar RCV:

RCV000013073

RCV000013074

RCV000147900

RCV000763480

RCV000999563

RCV001810853

RCV004540998

ClinVar Variation:

12281

HGVS (amino-acid)	Matching Registered Transcripts
NP_061966.1:p.Tyr487Asp	CA122080 NM_019093.4:c.1459T>G