Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699525C>T	CA256774	PRNP	c.305C>T (p.Pro102Leu) c.216C>T (p.Ala72=)	ClinVar dbSNP gnomAD v4
20	g.4699525C=	CA2347156493	PRNP	c.305C= (p.Pro102=) c.216C= (p.Ala72=)	dbSNP

Number of alleles fetched