A30P mutation

E1968043 UNEXPLORED

The A30P mutation is a pathogenic point mutation in the alpha-synuclein gene linked to familial forms of Parkinson’s disease.

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All labels observed (1)

Label Occurrences
A30P mutation canonical 1

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

alpha-synuclein → geneticVariantAssociatedWithDisease → A30P mutation ⓘ