Canonical Allele Identifier: PA2829969136
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 498022
ClinVar RCV Id: RCV000591349 RCV004543331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Val383Ile
CA2180020
NM_021027.3:c.1147G>A