Canonical Allele Identifier: PA2827182929
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 169
ClinVar RCV Id: RCV000000192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.Arg143Pro
CA113978
NM_001322971.2:c.428G>C