Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.49123179G>A	CA074319	LAMB2	c.4177C>T (p.Leu1393Phe) n.407C>T	ClinVar dbSNP gnomAD v2 gnomAD v4
3	g.49123179G=	CA1363340026	LAMB2	c.4177C= (p.Leu1393=) n.407C=	dbSNP

Number of alleles fetched