Allele Registry

Canonical Allele Identifier: PA122098

Gene: UGT1A4 HGNC NCBI

ClinVar RCV:

RCV000013076

RCV003488338

RCV003987318

ClinVar Variation:

12283

HGVS (amino-acid)	Matching Registered Transcripts
NP_009051.1:p.Gln358Arg	CA122091 NM_007120.3:c.1073A>G