Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
13	g.32338993dup	CA020568	BRCA2	c.4638dup (p.Asp1547Ter) c.4269dup (p.Asp1424Ter) n.4638dup	ClinVar dbSNP gnomAD v4
13	g.32338993del	CA020572	BRCA2	c.4638del (p.Phe1546LeufsTer22) c.4269del (p.Phe1423LeufsTer22) n.4638del	ClinVar dbSNP gnomAD v4

Number of alleles fetched