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Variant Information

Enter Variant:

Enter Gene:

Gene					Interpretation
MPL	chr1:43814979	chr1:43349308	c.1514G>A	p.S505N	Pathogenic
MPL	chr1:43815008	chr1:43349337	c.1543T>G	p.W515G	Pathogenic
MPL	chr1:43815009	chr1:43349338	c.1544G>C	p.W515S	Pathogenic