RS119103213 MCCC1
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What This Variant Does
"[OMIM:?]
Associated Conditions
3-methylcrotonyl-CoA carboxylase 1 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
3-methylcrotonyl-CoA carboxylase 1 deficiency
Methylcrotonyl-CoA carboxylase deficiency
Inborn genetic diseases
Other Variants in MCCC1