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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000475.1:p.Phe691Leu
NM_000484.4:c.2071T>C

NM_000484.4:c.2073T>A

NM_000484.4:c.2073T>G