Canonical Allele Identifier: PA916026775
Gene: OAT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309903.1:p.Tyr45Cys
CA113952
NM_001322974.2:c.134A>G