Canonical Allele Identifier: PA173887
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 160240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Ser250Pro
CA173885
NM_000463.3:c.748T>C