Allele Registry

Canonical Allele Identifier: PA122058

Gene: UGT1A7 HGNC NCBI

ClinVar RCV:

RCV000013060

RCV002247330

RCV003114188

ClinVar Variation:

12272

HGVS (amino-acid)	Matching Registered Transcripts
NP_061950.2:p.Gly305Glu	CA122054 NM_019077.3:c.914G>A