Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23425980C>A | CA389049034 | MYH7 | c.2146G>T (p.Gly716Trp) n.2252G>T | ClinVar dbSNP |
14 | g.23425980C>T | CA011770 | MYH7 | c.2146G>A (p.Gly716Arg) n.2252G>A | ClinVar dbSNP |
14 | g.23425980C>G | CA389049033 | MYH7 | c.2146G>C (p.Gly716Arg) n.2252G>C | ClinVar dbSNP |