Canonical Allele Identifier: PA916026770
Gene: OAT HGNC NCBI
ClinVar Allele:
15206
ClinVar RCV:
RCV000000190
ClinVar Variation:
167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.Ala77Thr
CA113971
NM_001322971.2:c.229G>A