Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.112450385G>A	CA354979	PTPN11	c.205G>A (p.Glu69Lys) c.202G>A (p.Glu68Lys)	ClinVar dbSNP COSMIC
12	g.112450385G>C	CA261565	PTPN11	c.205G>C (p.Glu69Gln) c.202G>C (p.Glu68Gln)	ClinVar dbSNP ExAC COSMIC

Number of alleles fetched