Allele Registry

Canonical Allele Identifier: PA122053

Gene: UGT1A1 HGNC NCBI

ClinVar RCV:

RCV000013059

RCV003556007

ClinVar Variation:

12271

HGVS (amino-acid)	Matching Registered Transcripts
NP_000454.1:p.Phe171del	CA122051 NM_000463.3:c.513_515del