Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47338519C>ACA012008MYBPC3c.2308+1G>T (p.=)
c.2290+1G>T (p.=)
c.2227+1G>T (p.=)
ClinVar dbSNP
11g.47338519C>TCA011996MYBPC3c.2308+1G>A (p.=)
c.2290+1G>A (p.=)
c.2227+1G>A (p.=)
ClinVar dbSNP
11g.47338519C>GCA221689791MYBPC3c.2308+1G>C (p.=)
c.2290+1G>C (p.=)
c.2227+1G>C (p.=)
dbSNP

Number of alleles fetched