Allele Registry

Canonical Allele Identifier: PA111932

Gene: UGT1A1 HGNC NCBI

ClinVar RCV:

RCV001808119

ClinVar Variation:

1333431

HGVS (amino-acid)	Matching Registered Transcripts
NP_000454.1:p.Gly276Arg	CA2179894 NM_000463.3:c.826G>C