Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38599020G>ACA16617953SCN5Ac.1921C>T (p.Gln641Ter)
c.1792C>T (p.Gln598Ter)
ClinVar dbSNP
3g.38599020G=CA1358581006SCN5Ac.1921C= (p.Gln641=)
c.1792C= (p.Gln598=)
dbSNP

Number of alleles fetched