Gene Mutations
 
Records Return:  (3) Show
 
GeneGene Omim NumberDisease Omim NumberChromosome LocationGene MutationAllelic VariantOmim PhenotypeSample Count
ENPP11733352080006q22-q23ASN792SER ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY2
ENPP11733352080006q22-q23PRO305THR ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY2
ENPP11733352080006q22-q23TYR312TER ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY2