Allele Registry

Canonical Allele Identifier: PA111899

Gene: UGT1A1 HGNC NCBI

ClinVar RCV:

RCV000013058

RCV001818152

ClinVar Variation:

12270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000454.1:p.Gln331Arg	CA122041 NM_000463.3:c.992A>G