Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
1	g.209633028C>T	CA257284	LAMB3	c.628+42G>A (n.628+42G>A) c.436+42G>A (n.436+42G>A)	ClinVar dbSNP gnomAD v3 gnomAD v4
1	g.209633028C=	CA1148224947	LAMB3	c.628+42G= (n.628+42G=) c.436+42G= (n.436+42G=)	dbSNP

Number of alleles fetched