Canonical Allele Identifier: PA916026768
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 56131
ClinVar RCV Id: RCV000049540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.Thr74Met
CA144165
NM_001322971.2:c.221C>T