Canonical Allele Identifier: PA112158
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597089
ClinVar RCV Id: RCV000733106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Trp354Arg
CA351073300
NM_000463.3:c.1060T>A
CA351073306
NM_000463.3:c.1060T>C