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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001372182.1:p.Phe634Leu
NM_001385253.1:c.1900T>C

NM_001385253.1:c.1902C>A

NM_001385253.1:c.1902C>G