Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110911094C>TCA010431MYL2c.484G>A (p.Gly162Arg)
c.427G>A (p.Gly143Arg)
c.442G>A (p.Gly148Arg)
 ClinVar dbSNP gnomAD v4 COSMIC
12g.110911094C>ACA386696715MYL2c.484G>T (p.Gly162Ter)
c.427G>T (p.Gly143Ter)
c.442G>T (p.Gly148Ter)
 ClinVar dbSNP

Number of alleles fetched