Canonical Allele Identifier: PA111971
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502841
ClinVar RCV Id: RCV003229499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Gly395Val
CA2180025
NM_000463.3:c.1184G>T