Canonical Allele Identifier: PA2579934061
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Glu693Asp
CA9987062
NM_000484.4:c.2079A>T
CA409805686
NM_000484.4:c.2079A>C