Canonical Allele Identifier: PA2827183072
Gene: OAT HGNC NCBI
ClinVar Allele:
15196
ClinVar RCV:
RCV000000180
ClinVar Variation:
157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.Pro310Leu
CA113943
NM_001322971.2:c.929C>T