ProCMD

ProCMD 3D protein C mutations database

Database for molecular aspects of thrombophilic disease. It integrates clinical and phenotypical descriptions with functional and structural data obtained by computational approach to help to elucidate the chain of events leading from the molecular defect to disease.

IDProCMD
Homehttp://www.itb.cnr.it/procmd/
EDAM topicHuman disease
EDAM topicDisease
EDAM topicGenotype and phenotype
TaxonHomo sapiens