Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
16	g.79599727G>T	CA214890	MAF	c.176C>A (p.Pro59His) n.2226C>A	ClinVar dbSNP
16	g.79599727G>A	CA175100	MAF	c.176C>T (p.Pro59Leu) n.2226C>T	ClinVar dbSNP
16	g.79599727G=	CA2235932810	MAF	c.176C= (p.Pro59=) n.2226C=	dbSNP

Number of alleles fetched