Canonical Allele Identifier: PA122011
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 12267
ClinVar RCV Id: RCV000013054 RCV001851815 RCV003387719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Ser372Phe
CA122007
NM_019076.5:c.1115C>T