Canonical Allele Identifier: PA354766
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Ala474Ser
CA249315
NM_021027.3:c.1420G>T