Canonical Allele Identifier: PA2829896619
Gene: UGT1A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061951.1:p.Ala478Ser
CA249315
NM_019078.2:c.1432G>T