Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
MT	m.9804G>A	CA340930	MT-CO3	c.598G>A (p.Ala200Thr)	ClinVar dbSNP
MT	m.9804G>C	CA414803748	MT-CO3	c.598G>C (p.Ala200Pro)	ClinVar dbSNP
MT	m.9804G>T	CA414803749	MT-CO3	c.598G>T (p.Ala200Ser)	ClinVar dbSNP

Number of alleles fetched