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中文
这种位于线粒体DNA第4739位的C到A的突变导致了从CTA密码子转换为miochondrial(甲基硫氨酸)密码子ATA，进而氨基酸位置276(记为p.L276M)上的Leucine变为 Methionine(甲硫氨酸)。这个改变发生在mitochondrial NADH dehydrogenase 2基因中(来源：J:97969)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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References Literature
Title
PMID
Journal
Year
IF
