Canonical Allele Identifier: PA113980
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 169
ClinVar RCV Id: RCV000000192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Arg112Pro
CA113978
NM_001171814.2:c.335G>C