Canonical Allele Identifier: PA916026772
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.Pro92Gln
CA114019
NM_001322971.2:c.275C>A