Allele Registry

Canonical Allele Identifier: PA113948

Gene: OAT HGNC NCBI

ClinVar RCV:

RCV000000181

RCV000049525

RCV000513174

ClinVar Variation:

158

56116

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165285.1:p.Leu299Phe	CA113946 NM_001171814.2:c.897G>C CA144141 NM_001171814.2:c.897G>T