Canonical Allele Identifier: PA2827183239
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1380528
ClinVar RCV Id: RCV001886385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309903.1:p.Asn200Tyr
CA378633202
NM_001322974.2:c.598A>T