Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23432656T>CCA16042917MYH7c.485A>G (p.Tyr162Cys)
n.591A>G
ClinVar dbSNP
14g.23432656T=CA2123454008MYH7c.485A= (p.Tyr162=)
n.591A=
dbSNP

Number of alleles fetched