Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.31820357C>A	CA116736	MYLK2	c.284C>A (p.Ala95Glu) n.449C>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20	g.31820357C=	CA2360015493	MYLK2	c.284C= (p.Ala95=) n.449C=	dbSNP

Number of alleles fetched