Canonical Allele Identifier: PA2828960658
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Lys454Asn
CA9987289
NM_001385253.1:c.1362G>C
CA409810300
NM_001385253.1:c.1362G>T