Allele Registry

Canonical Allele Identifier: PA122096

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000013076

RCV003488338

RCV003987318

ClinVar Variation:

12283

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Gln354Arg	CA122091 NM_021027.3:c.1061A>G