Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.46859509C>ACA013830MYL3c.447G>T (p.Met149Ile)
n.669G>T
n.405G>T
 ClinVar dbSNP COSMIC
3g.46859509C>TCA013812MYL3c.447G>A (p.Met149Ile)
n.669G>A
n.405G>A
 ClinVar dbSNP

Number of alleles fetched