Canonical Allele Identifier: PA2829896085
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502841
ClinVar RCV Id: RCV003229499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Gly392Val
CA2180025
NM_019076.5:c.1175G>T