Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110915771T>CCA009842MYL2c.113A>G (p.Gln38Arg)
c.56A>G (p.Gln19Arg)
c.94-1447A>G (n.94-1447A>G)
 ClinVar dbSNP
12g.110915771T=CA2063075003MYL2c.113A= (p.Gln38=)
c.56A= (p.Gln19=)
c.94-1447A= (n.94-1447A=)
 dbSNP

Number of alleles fetched