Canonical Allele Identifier: PA113942
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 156
ClinVar RCV Id: RCV000000179 RCV002509140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Leu264Pro
CA113940
NM_001171814.2:c.791T>C