Allele Registry

Canonical Allele Identifier: PA209154

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000194762

RCV000300556

RCV000763479

RCV000999562

RCV001250229

RCV003987438

RCV004530149

ClinVar Variation:

212543

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Pro361Leu	CA209149 NM_021027.3:c.1082C>T