Gene Mutations
 
Records Return:  (2) Show
 
GeneGene Omim NumberDisease Omim NumberChromosome LocationGene MutationAllelic VariantOmim PhenotypeSample Count
ALG66045666031471p22.3897_899delAAT CONGENITAL DISORDER OF GLYCOSYLATION; TYPE Ic1
ALG66045666031471p22.3IVS7+2T>G CONGENITAL DISORDER OF GLYCOSYLATION; TYPE Ic1