Allele Registry

Canonical Allele Identifier: PA111835

Gene: UGT1A1 HGNC NCBI

ClinVar Variation Id: 288098

HGVS (amino-acid)	Matching Registered Transcripts
NP_000454.1:p.Arg367Cys	CA2180010 NM_000463.3:c.1099C>T