Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110913324C>ACA010026MYL2c.275G>T (p.Gly92Val)
c.218G>T (p.Gly73Val)
c.233G>T (p.Gly78Val)
n.106G>T
 ClinVar dbSNP
12g.110913324C>TCA386698175MYL2c.275G>A (p.Gly92Glu)
c.218G>A (p.Gly73Glu)
c.233G>A (p.Gly78Glu)
n.106G>A
 ClinVar dbSNP

Number of alleles fetched