Allele Registry

Canonical Allele Identifier: PA111979

Gene: UGT1A4 HGNC NCBI

ClinVar RCV:

RCV000013058

RCV001818152

ClinVar Variation:

12270

HGVS (amino-acid)	Matching Registered Transcripts
NP_009051.1:p.Gln332Arg	CA122041 NM_007120.3:c.995A>G