Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.157770385C>ACA16602803ACVR1c.773G>T (p.Arg258Met)
n.790G>T
n.981G>T
ClinVar dbSNP COSMIC
2g.157770385C=CA1301098262ACVR1c.773G= (p.Arg258=)
n.790G=
n.981G=
dbSNP

Number of alleles fetched