Canonical Allele Identifier: PA113939
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Arg133Lys
CA113937
NM_001171814.2:c.398G>A