Canonical Allele Identifier: PA2827181394
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 56140
ClinVar RCV Id: RCV000049549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309895.1:p.Asn326Lys
CA144186
NM_001322966.2:c.978T>A
CA378633961
NM_001322966.2:c.978T>G