Canonical Allele Identifier: PA2826270557
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Lys491Asn
CA9987289
NM_001204302.2:c.1473G>C
CA409810300
NM_001204302.2:c.1473G>T