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This allele is not present in the registry. To get a canonical identifier, please click on the "Get identifier" below.
Canonical Allele Identifier:
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Gene: APP
HGNC
NCBI
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001191232.1:p.Lys577_Met578delinsAsnLeu
NM_001204303.2:c.[1731G>C;1732A>C]
NM_001204303.2:c.[1731G>C;1732A>T]
NM_001204303.2:c.[1731G>T;1732A>C]
NM_001204303.2:c.[1731G>T;1732A>T]
NM_001204303.2:c.1731_1732delinsTC
