Canonical Allele Identifier: PA2579933487
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Ile712Leu
CA409805573
NM_000484.4:c.2134A>T
CA409805575
NM_000484.4:c.2134A>C