Canonical Allele Identifier: PA2827182030
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1371153
ClinVar RCV Id: RCV001864457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Ala214Ser
CA378636102
NM_001322968.2:c.640G>T