Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47338646C>ACA011848MYBPC3c.2182G>T (p.Glu728Ter)
c.2164G>T (p.Glu722Ter)
c.2101G>T (p.Glu701Ter)
 ClinVar dbSNP gnomAD v4
11g.47338646C=CA1969332499MYBPC3c.2182G= (p.Glu728=)
c.2164G= (p.Glu722=)
c.2101G= (p.Glu701=)
 dbSNP

Number of alleles fetched