Allele Registry

Canonical Allele Identifier: PA209152

Gene: UGT1A8 HGNC NCBI

ClinVar RCV:

RCV000194762

RCV000300556

RCV000763479

RCV000999562

RCV001250229

RCV003987438

RCV004530149

ClinVar Variation:

212543

HGVS (amino-acid)	Matching Registered Transcripts
NP_061949.3:p.Pro361Leu	CA209149 NM_019076.5:c.1082C>T