After more than 15 years the Human Cytochrome
P450 (CYP) Allele Nomenclature Database has transitioned…
…to the Pharmacogene Variation (PharmVar) Consortium at www.PharmVar.org
PharmVar will serve as a central repository for pharmacogene variation to facilitate
allele (haplotype) designation and the interpretation of pharmacogenetic test results to guide precision medicine
PharmVar is a PGRN resource funded by NIGMS.
After September 26, 2017, please visit www.PharmVar.org to access content of the original
P450 Nomenclature Database