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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Thr719Ser
CA409805538
NM_000484.4:c.2156C>G
CA409805540
NM_000484.4:c.2155A>T