Canonical Allele Identifier: PA2827181631
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 56131
ClinVar RCV Id: RCV000049540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309896.1:p.Thr181Met
CA144165
NM_001322967.2:c.542C>T