GENETIC ENCYCLOPEDIA
ABOUT US
disease: Apolipoprotein C2 deficiency
id
323
name
Apolipoprotein C2 deficiency
variant-disease
NM_000483.5(APOC2):c.55+1G>C AND Apolipoprotein C2 deficiency
NM_000483.5(APOC2):c.*116T>C AND Apolipoprotein C2 deficiency
NM_000483.5(APOC2):c.*203G>A AND Apolipoprotein C2 deficiency
NM_000483.5(APOC2):c.-2C>T AND Apolipoprotein C2 deficiency
APOC2, 1-BP INS AND Apolipoprotein C2 deficiency
... 19 more