Canonical Allele Identifier: PA112202
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 160239
ClinVar RCV Id: RCV000147904 RCV000313763 RCV000396791 RCV000348706 RCV000592026 RCV001004164 RCV004532664 RCV002514850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Val225Gly
CA173883
NM_000463.3:c.674T>G