Canonical Allele Identifier: PA2827182052
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 160
ClinVar RCV Id: RCV000000183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Tyr245Cys
CA113952
NM_001322968.2:c.734A>G