Allele Registry

Canonical Allele Identifier: PA122046

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000013058

RCV001818152

ClinVar Variation:

12270

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Gln328Arg	CA122041 NM_021027.3:c.983A>G