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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Val697Leu
CA409805527
NM_001136016.3:c.2089G>T
CA409805528
NM_001136016.3:c.2089G>C