Canonical Allele Identifier: PA2829896065
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 593490
ClinVar RCV Id: RCV000728545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Arg364Leu
CA2180012
NM_019076.5:c.1091G>T