Allele Registry

Canonical Allele Identifier: PA122099

Gene: UGT1A5 HGNC NCBI

ClinVar RCV:

RCV000013076

RCV003488338

RCV003987318

ClinVar Variation:

12283

HGVS (amino-acid)	Matching Registered Transcripts
NP_061951.1:p.Gln358Arg	CA122091 NM_019078.2:c.1073A>G