Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.174729222C>TCA251352MSX2c.443C>T (p.Pro148Leu)
c.*67C>T (n.*67C>T)
ClinVar dbSNP
5g.174729222C>ACA341436MSX2c.443C>A (p.Pro148His)
c.*67C>A (n.*67C>A)
ClinVar dbSNP

Number of alleles fetched