Canonical Allele Identifier: PA122059
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 12272
ClinVar RCV Id: RCV000013060 RCV002247330 RCV003114188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Gly305Glu
CA122054
NM_021027.3:c.914G>A