Canonical Allele Identifier: PA2827182113
Gene: OAT HGNC NCBI
ClinVar RCV:
RCV000000187
ClinVar Variation:
164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.His319Tyr
CA113964
NM_001322968.2:c.955C>T