Canonical Allele Identifier: PA2579986259
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Leu688Phe
CA409806207
NM_000484.4:c.2064G>T
CA409806208
NM_000484.4:c.2064G>C