Amino acid replacement: V423E.
T8067576A
V423E | mys-PA; V423E | mys-PB; V423E | mys-PC; V423E | mys-PD
V423E
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Strong allele.
Selected as: a mutation that permits the survival of an F1 male.