Canonical Allele Identifier: PA2827182629
Gene: OAT HGNC NCBI
ClinVar RCV:
RCV000000186
ClinVar Variation:
163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309899.1:p.Asn54Lys
CA113962
NM_001322970.2:c.162C>A
CA378638056
NM_001322970.2:c.162C>G