Canonical Allele Identifier: PA645438099
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 437207
ClinVar RCV Id: RCV000501526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Ser198Pro
CA351067297
NM_000463.3:c.592T>C