Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225605T>C	CA125120	HBB	c.437A>G (p.Tyr146Cys) c.253A>G (n.253A>G)	ClinVar dbSNP
11	g.5225605T=	CA1949564107	HBB	c.437A= (p.Tyr146=) c.253A= (n.253A=)	dbSNP

Number of alleles fetched