Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.54277981C>GCA16602385PDGFRAc.1977C>G (p.Asn659Lys)
n.215C>G
c.1257C>G (p.Asn419Lys)
n.403C>G
n.1795C>G
c.2052C>G (p.Asn684Lys)
c.2016C>G (p.Asn672Lys)
ClinVar dbSNP COSMIC
4g.54277981C>ACA16602384PDGFRAc.1977C>A (p.Asn659Lys)
n.215C>A
c.1257C>A (p.Asn419Lys)
n.403C>A
n.1795C>A
c.2052C>A (p.Asn684Lys)
c.2016C>A (p.Asn672Lys)
ClinVar dbSNP COSMIC

Number of alleles fetched