Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23417598G>TCA485617833MYH7c.4258C>A (p.Arg1420=)
 ClinVar dbSNP gnomAD v4
14g.23417598G>ACA014718MYH7c.4258C>T (p.Arg1420Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched