Canonical Allele Identifier: PA2825817788
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Lys379Asn
CA9987289
NM_001136129.3:c.1137G>C
CA409810300
NM_001136129.3:c.1137G>T