Canonical Allele Identifier: PA113974
Gene: OAT HGNC NCBI
ClinVar RCV:
RCV000000190
ClinVar Variation:
167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Ala46Thr
CA113971
NM_001171814.2:c.136G>A