Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
MT	m.9478T>G	CA414803031	MT-CO3	c.272T>G (p.Val91Gly)	ClinVar dbSNP
MT	m.9478T>C	CA345915	MT-CO3	c.272T>C (p.Val91Ala)	ClinVar dbSNP

Number of alleles fetched