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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.52519741C>T
CA10588554
KRT5
c.555+1G>A (n.555+1G>A)
c.225+1G>A (n.225+1G>A)
n.653+1G>A
ClinVar
dbSNP
12
g.52519741C=
CA2036540420
KRT5
c.555+1G= (n.555+1G=)
c.225+1G= (n.225+1G=)
n.653+1G=
dbSNP
Number of alleles fetched
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