Canonical Allele Identifier: PA114021
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165285.1:p.Pro61Gln
CA114019
NM_001171814.2:c.182C>A