Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.46859505C>TCA352093MYL3c.451G>A (p.Ala151Thr)
n.673G>A
n.409G>A
 ClinVar dbSNP
3g.46859505C=CA1362297090MYL3c.451G= (p.Ala151=)
n.673G=
n.409G=
 dbSNP

Number of alleles fetched