Canonical Allele Identifier: PA2825146882
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Ala477Ser
CA249315
NM_000463.3:c.1429G>T