Canonical Allele Identifier: PA2827181749
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309896.1:p.His319Tyr
CA113964
NM_001322967.2:c.955C>T