Canonical Allele Identifier: PA113966
Gene: OAT HGNC NCBI
ClinVar RCV:
RCV000000187
ClinVar Variation:
164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.His181Tyr
CA113964
NM_001171814.2:c.541C>T