Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23425772C>ACA16619852MYH7c.2209G>T (p.Asp737Tyr)
n.2315G>T
ClinVar dbSNP
14g.23425772C=CA2123458427MYH7c.2209G= (p.Asp737=)
n.2315G=
dbSNP

Number of alleles fetched