Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.120446304C>T	CA333675	LAMP2	c.864+1G>A (n.864+1G>A) c.407+1G>A	ClinVar dbSNP
X	g.120446304C>A	CA176520	LAMP2	c.864+1G>T (n.864+1G>T) c.407+1G>T	ClinVar dbSNP
X	g.120446304C=	CA2454872269	LAMP2	c.864+1G= (n.864+1G=) c.407+1G=	dbSNP

Number of alleles fetched