Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112450395C>ACA16602941PTPN11c.215C>A (p.Ala72Asp)
c.212C>A (p.Ala71Asp)
ClinVar dbSNP COSMIC
12g.112450395C>GCA235319PTPN11c.215C>G (p.Ala72Gly)
c.212C>G (p.Ala71Gly)
ClinVar dbSNP COSMIC
12g.112450395C>TCA215451PTPN11c.215C>T (p.Ala72Val)
c.212C>T (p.Ala71Val)
ClinVar dbSNP COSMIC
12g.112450395C=CA2063740202PTPN11c.215C= (p.Ala72=)
c.212C= (p.Ala71=)
dbSNP

Number of alleles fetched