Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23425997G>ACA011756MYH7c.2129C>T (p.Pro710Leu)
n.2235C>T
 ClinVar dbSNP
14g.23425997G>TCA011747MYH7c.2129C>A (p.Pro710His)
n.2235C>A
 ClinVar dbSNP

Number of alleles fetched