Canonical Allele Identifier: PA658803389
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 498022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Val386Ile
CA2180020
NM_000463.3:c.1156G>A