Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699600G>T	CA123099	PRNP	c.380G>T (p.Gly127Val) c.69G>T (n.69G>T)	ClinVar dbSNP gnomAD v2 gnomAD v4
20	g.4699600G=	CA2347156520	PRNP	c.380G= (p.Gly127=) c.69G= (n.69G=)	dbSNP

Number of alleles fetched