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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.70027956C>T
CA181048
EDA
c.626C>T (p.Pro209Leu)
c.230C>T (p.Pro77Leu)
ClinVar
dbSNP
X
g.70027956C=
CA2435979586
EDA
c.626C= (p.Pro209=)
c.230C= (p.Pro77=)
dbSNP
Number of alleles fetched
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