Canonical Allele Identifier: PA173882
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 160238
ClinVar RCV Id: RCV000147903 RCV001450052
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Val160Glu
CA173880
NM_000463.3:c.479T>A