Canonical Allele Identifier: PA122062
Gene: UGT1A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 12272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061951.1:p.Gly309Glu
CA122054
NM_019078.2:c.926G>A