Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110911090T>CCA010454MYL2c.488A>G (p.Glu163Gly)
c.431A>G (p.Glu144Gly)
c.446A>G (p.Glu149Gly)
 ClinVar dbSNP
12g.110911090T>GCA010447MYL2c.488A>C (p.Glu163Ala)
c.431A>C (p.Glu144Ala)
c.446A>C (p.Glu149Ala)
 ClinVar dbSNP

Number of alleles fetched