Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23426003C>GCA011730MYH7c.2123G>C (p.Gly708Ala)
n.2229G>C
 ClinVar dbSNP
14g.23426003C>ACA011739MYH7c.2123G>T (p.Gly708Val)
n.2229G>T
 ClinVar dbSNP

Number of alleles fetched