Canonical Allele Identifier: PA103940
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000265.1:p.His319Tyr
CA113964
NM_000274.4:c.955C>T