RS74315297 CPT2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
neonatal form
myopathic form
severe infantile form
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
neonatal form
myopathic form
severe infantile form
Other Variants in CPT2