Canonical Allele Identifier: PA2829969185
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2412815
ClinVar RCV Id: RCV003108246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Arg447Leu
CA67599434
NM_021027.3:c.1340G>T