Canonical Allele Identifier: PA245935
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 197672
ClinVar RCV Id: RCV000178772 RCV002478593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Pro448Leu
CA245929
NM_021027.3:c.1343C>T