Canonical Allele Identifier: PA2579933558
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000475.1:p.Phe690Leu
NM_000484.4:c.2068T>C

NM_000484.4:c.2070C>A

NM_000484.4:c.2070C>G