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
ENSP00000350578.3:p.Lys651_Met652delinsAsnLeu
ENST00000357903.7:c.[1953G>C;1954A>C]
ENST00000357903.7:c.[1953G>C;1954A>T]
ENST00000357903.7:c.[1953G>T;1954A>C]
ENST00000357903.7:c.[1953G>T;1954A>T]
ENST00000357903.7:c.1953_1954delinsTC
