Canonical Allele Identifier: PA113936
Gene: OAT HGNC NCBI
ClinVar Allele:
15193
ClinVar RCV:
RCV000000177
ClinVar Variation:
154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Ala132Pro
CA113934
NM_001171814.2:c.394G>C