clingenPreferredTitle
is now communityStandardTitle
Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.9698T>G | CA337098536 | n.492T>G (p.Leu164=) | dbSNP | |
MT | m.9698T>C | CA337098533 | n.492T>C (p.Leu164=) | dbSNP | |
MT | m.9698T>A | CA337098529 | n.492T>A (p.Leu164=) | dbSNP |