Canonical Allele Identifier: PA2829896049
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 597089
ClinVar RCV Id: RCV000733106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Trp351Arg
CA351073300
NM_019076.5:c.1051T>A
CA351073306
NM_019076.5:c.1051T>C