Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
1	g.114716127C>A	CA297020	NRAS	c.34G>T (p.Gly12Cys)	ClinVar dbSNP COSMIC
1	g.114716127C>G	CA297030	NRAS	c.34G>C (p.Gly12Arg)	ClinVar dbSNP COSMIC
1	g.114716127C>T	CA180753	NRAS	c.34G>A (p.Gly12Ser)	ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched