Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110911096T>CCA010425MYL2c.482A>G (p.His161Arg)
c.425A>G (p.His142Arg)
c.440A>G (p.His147Arg)
 ClinVar dbSNP
12g.110911096T=CA2063066665MYL2c.482A= (p.His161=)
c.425A= (p.His142=)
c.440A= (p.His147=)
 dbSNP

Number of alleles fetched