Canonical Allele Identifier: PA127796
Gene: APP HGNC NCBI

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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000475.1:p.Lys670_Met671delinsAsnLeu
NM_000484.4:c.[2010G>C;2011A>C]

NM_000484.4:c.[2010G>C;2011A>T]

NM_000484.4:c.[2010G>T;2011A>C]

NM_000484.4:c.[2010G>T;2011A>T]

NM_000484.4:c.2010_2011delinsTC