Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
MT	m.3796A>T	CA10581388	MT-ND1	c.490A>T (p.Thr164Ser)	ClinVar dbSNP
MT	m.3796A>G	CA340947	MT-ND1	c.490A>G (p.Thr164Ala)	ClinVar dbSNP

Number of alleles fetched