Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.130208685G>A	CA151132	ST14	c.2269+1G>A (n.2269+1G>A)	ClinVar dbSNP
11	g.130208685G=	CA2008890251	ST14	c.2269+1G= (n.2269+1G=)	dbSNP

Number of alleles fetched