Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47342697C>ACA010518MYBPC3c.1505G>T (p.Arg502Leu)
c.1487G>T (p.Arg496Leu)
ClinVar dbSNP
11g.47342697C>TCA010508MYBPC3c.1505G>A (p.Arg502Gln)
c.1487G>A (p.Arg496Gln)
ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched