Canonical Allele Identifier: PA2825398842
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 597089
ClinVar RCV Id: RCV000733106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001063.2:p.Trp353Arg
CA351073300
NM_001072.4:c.1057T>A
CA351073306
NM_001072.4:c.1057T>C