Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.189868639A>TCA355755209TP63c.1052A>T (p.Asp351Val)
c.770A>T (p.Asp257Val)
c.515A>T (p.Asp172Val)
n.876A>T
c.1001A>T (p.Asp334Val)
c.1049A>T (p.Asp350Val)
c.1046A>T (p.Asp349Val)
c.1013A>T (p.Asp338Val)
dbSNP
3g.189868639A>GCA118341TP63c.1052A>G (p.Asp351Gly)
c.770A>G (p.Asp257Gly)
c.515A>G (p.Asp172Gly)
n.876A>G
c.1001A>G (p.Asp334Gly)
c.1049A>G (p.Asp350Gly)
c.1046A>G (p.Asp349Gly)
c.1013A>G (p.Asp338Gly)
ClinVar dbSNP

Number of alleles fetched