Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23415212C>ACA389035775MYH7c.5342G>T (p.Arg1781Leu)
 ClinVar dbSNP
14g.23415212C>TCA015985MYH7c.5342G>A (p.Arg1781His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415212C=CA2123462451MYH7c.5342G= (p.Arg1781=)
 dbSNP

Number of alleles fetched