Allele Registry

Canonical Allele Identifier: PA122086

Gene: UGT1A9 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

27320

ClinVar RCV:

RCV000013073

RCV000013074

RCV000147900

RCV000763480

RCV000999563

RCV001810853

RCV004540998

ClinVar Variation:

12281

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Tyr483Asp	CA122080 NM_021027.3:c.1447T>G