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Mutations on the Protein: Q92743 From Positions: 288 To 312

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Swiss-Prot Disease: VAR_063149
p.VAL297MET
N/A
N/A
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, autosomal recessive (CARASIL)


OMIM Disease: 602194.0003
p.ARG302TER
N/A
N/A
CEREBRAL AUTOSOMAL RECESSIVE ARTERIOPATHY WITH SUBCORTICAL INFARCTS||AND LEUKOENCEPHALOPATHY


OMIM Disease: 602194.0006
p.GLY295ARG
N/A
N/A
CEREBRAL AUTOSOMAL RECESSIVE ARTERIOPATHY WITH SUBCORTICAL INFARCTS||AND LEUKOENCEPHALOPATHY


OMIM Disease: 602194.0004
p.VAL297MET
N/A
N/A
CEREBRAL AUTOSOMAL RECESSIVE ARTERIOPATHY WITH SUBCORTICAL INFARCTS||AND LEUKOENCEPHALOPATHY






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