Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23424815A>GCA16614088MYH7c.2633T>C (p.Val878Ala)
n.2739T>C
ClinVar dbSNP
14g.23424815A=CA2123455797MYH7c.2633T= (p.Val878=)
n.2739T=
dbSNP

Number of alleles fetched