Canonical Allele Identifier: PA2827182050
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309897.1:p.Pro241Leu
CA113975
NM_001322968.2:c.722C>T