Canonical Allele Identifier: PA913193266
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597250
ClinVar RCV Id: RCV000733308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Pro387Arg
CA351074205
NM_000463.3:c.1160C>G
CA913189479
NM_000463.3:c.1160_1161delinsGT