Canonical Allele Identifier: PA2829687593
Gene: UGT1A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 218786
ClinVar RCV Id: RCV000203111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009051.1:p.Ala478Ser
CA249315
NM_007120.3:c.1432G>T