ClinGen Allele Registry
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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_001129603.1:p.Lys560_Met561delinsAsnLeu
NM_001136131.2:c.[1680G>C;1681A>C]
NM_001136131.2:c.[1680G>C;1681A>T]
NM_001136131.2:c.[1680G>T;1681A>C]
NM_001136131.2:c.[1680G>T;1681A>T]
NM_001136131.2:c.1680_1681delinsTC
