Canonical Allele Identifier: PA2829896141
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Ala474Ser
CA249315
NM_019076.5:c.1420G>T