Canonical Allele Identifier: PA2827181386
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309895.1:p.His319Tyr
CA113964
NM_001322966.2:c.955C>T