Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699818G>A	CA256778	PRNP	c.598G>A (p.Glu200Lys) c.287G>A (n.287G>A)	ClinVar dbSNP gnomAD v2 gnomAD v4
20	g.4699818G=	CA2347156626	PRNP	c.598G= (p.Glu200=) c.287G= (n.287G=)	dbSNP

Number of alleles fetched