Canonical Allele Identifier: PA111801
Gene: UGT1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 437211
ClinVar RCV Id: RCV000503589 RCV000623653 RCV002508784 RCV004527613 RCV001727734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000454.1:p.Arg209Trp
CA2179856
NM_000463.3:c.625C>T