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中文
这个名为rs27680364的C变异类型，它编码的是阿尔法氨基酸（alanine）的529位，存在于以下品种中：A/J、AKR/J、C3H/HeJ、DBA/1J、DBA/2J、KK/HlJ、MOLF/EiJ、PWD/PhJ、PWK/PhJ、RIIIIS/J、SPRET/EiJ和ST/bJ（参考文献：J:179572）。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
