Canonical Allele Identifier: PA122063
Gene: UGT1A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 12272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061966.1:p.Gly309Glu
CA122054
NM_019093.4:c.926G>A