Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.123642468G>C	CA10575989	SCN3B	c.423C>G (p.Ile141Met) c.119C>G n.830C>G	ClinVar dbSNP gnomAD v4 COSMIC
11	g.123642468G>A	CA477241014	SCN3B	c.423C>T (p.Ile141=) c.119C>T n.830C>T	ClinVar dbSNP gnomAD v4

Number of alleles fetched