Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.211702102C>ACA350442465ERBB4c.1354G>T (p.Glu452Ter)
c.1276G>T (p.Glu426Ter)
c.1353G>T
c.1177G>T (p.Glu393Ter)
n.1406G>T
c.1432G>T (p.Glu478Ter)
c.733G>T (p.Glu245Ter)
dbSNP
2g.211702102C>TCA16602262ERBB4c.1354G>A (p.Glu452Lys)
c.1276G>A (p.Glu426Lys)
c.1353G>A
c.1177G>A (p.Glu393Lys)
n.1406G>A
c.1432G>A (p.Glu478Lys)
c.733G>A (p.Glu245Lys)
ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched