Allele Registry

Canonical Allele Identifier: PA2829969109

Gene: UGT1A9 HGNC NCBI

ClinVar RCV:

RCV000595778

RCV004543322

ClinVar Variation:

497628

HGVS (amino-acid)	Matching Registered Transcripts
NP_066307.1:p.Gly359Val	CA2180005 NM_021027.3:c.1076G>T