Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
1	g.209650120T>C	CA273899	LAMB3	c.29-2A>G (n.29-2A>G)	ClinVar dbSNP gnomAD v2 gnomAD v4
1	g.209650120T=	CA1143784366	LAMB3	c.29-2A= (n.29-2A=)	dbSNP

Number of alleles fetched