Canonical Allele Identifier: PA2827181689
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 160
ClinVar RCV Id: RCV000000183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309896.1:p.Tyr245Cys
CA113952
NM_001322967.2:c.734A>G