Canonical Allele Identifier: PA3088543200
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Met722Leu
CA409805521
NM_000484.4:c.2164A>T
CA409805523
NM_000484.4:c.2164A>C