RS150591260 MCCC2
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What This Variant Does
"CLNSIG=255
Associated Conditions
3-methylcrotonyl-CoA carboxylase 2 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
See cases
MCCC2-related disorder
3-methylcrotonyl-CoA carboxylase 2 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
See cases
MCCC2-related disorder
Other Variants in MCCC2