Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23393437C>TCA389010892MYH6c.3010G>A (p.Ala1004Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23393437C>ACA134311MYH6c.3010G>T (p.Ala1004Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23393437C=CA2123413764MYH6c.3010G= (p.Ala1004=)
dbSNP

Number of alleles fetched