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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001129602.1:p.Lys614_Met615delinsAsnLeu
NM_001136130.2:c.[1842G>C;1843A>C]

NM_001136130.2:c.[1842G>C;1843A>T]

NM_001136130.2:c.[1842G>T;1843A>C]

NM_001136130.2:c.[1842G>T;1843A>T]

NM_001136130.2:c.1842_1843delinsTC