Canonical Allele Identifier: PA2827182986
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309900.1:p.His212Tyr
CA113964
NM_001322971.2:c.634C>T