Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
1	g.114716124C>G	CA151261	NRAS	c.37G>C (p.Gly13Arg)	ClinVar dbSNP gnomAD v4 COSMIC
1	g.114716124C>A	CA16602248	NRAS	c.37G>T (p.Gly13Cys)	ClinVar dbSNP gnomAD v4 COSMIC
1	g.114716124C>T	CA16602674	NRAS	c.37G>A (p.Gly13Ser)	ClinVar dbSNP COSMIC

Number of alleles fetched