Canonical Allele Identifier: PA2825398898
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709802
ClinVar RCV Id: RCV002290144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001063.2:p.Arg402Leu
CA351074944
NM_001072.4:c.1205G>T