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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
5
g.174729222C>T
CA251352
MSX2
c.443C>T (p.Pro148Leu)
c.*67C>T (n.*67C>T)
ClinVar
dbSNP
5
g.174729222C>A
CA341436
MSX2
c.443C>A (p.Pro148His)
c.*67C>A (n.*67C>A)
ClinVar
dbSNP
Number of alleles fetched
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