[Term]
id: PR:000026117
name: methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant (human)
def: "A methylcrotonoyl-CoA carboxylase beta chain, mitochondrial (human) that has at least one amino acid residue that differs from the corresponding residue found in another methylcrotonoyl-CoA carboxylase beta chain, mitochondrial (human) when such a difference arises as the result of genetic differences, i.e., different alleles of methylcrotonoyl-CoA carboxylase beta chain, mitochondrial (human). Operationally, this means the sequence representation of the methylcrotonoyl-CoA carboxylase beta chain, mitochondrial(human) has at least one amino acid residue that differs from the corresponding residue found in the sequence represented by UniProtKB:Q9HCC0-1." [PRO:CNA]
comment: Category=organism-sequence.
synonym: "hMCCC2/var+" EXACT PRO-short-label [PRO:DNx]
is_a: PR:Q9HCC0 ! methylcrotonoyl-CoA carboxylase beta chain, mitochondrial (human)
relationship: only_in_taxon NCBITaxon:9606 ! Homo sapiens