Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38604007A>CCA015051SCN5Ac.1595T>G (p.Phe532Cys)
c.1466T>G (p.Phe489Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38604007A=CA1358585006SCN5Ac.1595T= (p.Phe532=)
c.1466T= (p.Phe489=)
dbSNP

Number of alleles fetched