Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4862808C>TCA124426MSX1c.577C>T (p.Gln193Ter)
n.289C>T
 ClinVar dbSNP
4g.4862808C=CA1435013661MSX1c.577C= (p.Gln193=)
n.289C=
 dbSNP

Number of alleles fetched