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
ENSP00000398879.2:p.Lys614_Met615delinsAsnLeu
ENST00000439274.6:c.[1842G>C;1843A>C]
ENST00000439274.6:c.[1842G>C;1843A>T]
ENST00000439274.6:c.[1842G>T;1843A>C]
ENST00000439274.6:c.[1842G>T;1843A>T]
ENST00000439274.6:c.1842_1843delinsTC