Allele Registry

Canonical Allele Identifier: PA2829969107

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000482866

RCV004527589

ClinVar Variation:

420162

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Gly359Ser	CA2179986 NM_021027.3:c.1075G>A