Canonical Allele Identifier: PA916026774
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309903.1:p.Pro41Leu
CA113975
NM_001322974.2:c.122C>T