Canonical Allele Identifier: PA3088543212
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Val736Leu
CA409805423
NM_000484.4:c.2206G>T
CA409805424
NM_000484.4:c.2206G>C