Canonical Allele Identifier: PA2827182120
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 56140
ClinVar RCV Id: RCV000049549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Asn326Lys
CA144186
NM_001322968.2:c.978T>A
CA378633961
NM_001322968.2:c.978T>G