Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23425980C>ACA389049034MYH7c.2146G>T (p.Gly716Trp)
n.2252G>T
ClinVar dbSNP
14g.23425980C>TCA011770MYH7c.2146G>A (p.Gly716Arg)
n.2252G>A
ClinVar dbSNP
14g.23425980C>GCA389049033MYH7c.2146G>C (p.Gly716Arg)
n.2252G>C
ClinVar dbSNP

Number of alleles fetched