Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
MT	m.14484T>C	CA340932	MT-ND6	c.190A>G (p.Met64Val)	ClinVar dbSNP
MT	m.14484T>G	CA414822695	MT-ND6	c.190A>C (p.Met64Leu)	ClinVar dbSNP

Number of alleles fetched