Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
5	g.70942416C>G	CA254692	SMN1	c.332C>G (p.Ala111Gly) c.274-302C>G (n.274-302C>G)	ClinVar dbSNP
5	g.70942416C=	CA1554171491	SMN1	c.332C= (p.Ala111=) c.274-302C= (n.274-302C=)	dbSNP

Number of alleles fetched