Canonical Allele Identifier: PA2827182071
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 56136
ClinVar RCV Id: RCV000049545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Thr267Ile
CA144180
NM_001322968.2:c.800C>T