Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47342627A>TCA079297MYBPC3c.1575T>A (p.Tyr525Ter)
c.1557T>A (p.Tyr519Ter)
 ClinVar dbSNP gnomAD v4
11g.47342627A>CCA010653MYBPC3c.1575T>G (p.Tyr525Ter)
c.1557T>G (p.Tyr519Ter)
 ClinVar dbSNP

Number of alleles fetched