Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112450352A>TCA297070PTPN11c.172A>T (p.Asn58Tyr)
c.169A>T (p.Asn57Tyr)
ClinVar dbSNP COSMIC
12g.112450352A>GCA261558PTPN11c.172A>G (p.Asn58Asp)
c.169A>G (p.Asn57Asp)
ClinVar dbSNP
12g.112450352A>CCA235310PTPN11c.172A>C (p.Asn58His)
c.169A>C (p.Asn57His)
ClinVar dbSNP

Number of alleles fetched