Canonical Allele Identifier: PA2827181990
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 878554
ClinVar RCV Id: RCV001105245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Trp178Ser
CA378636717
NM_001322968.2:c.533G>C