Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
14	g.23425970C>T	CA011785	MYH7	c.2156G>A (p.Arg719Gln) n.2262G>A	ClinVar dbSNP
14	g.23425970C>G	CA277665	MYH7	c.2156G>C (p.Arg719Pro) n.2262G>C	ClinVar dbSNP
14	g.23425970C=	CA2123459095	MYH7	c.2156G= (p.Arg719=) n.2262G=	dbSNP

Number of alleles fetched