Canonical Allele Identifier: PA113961
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Val194Met
CA113959
NM_001171814.2:c.580G>A