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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Val613Leu
CA409806469
NM_001136130.2:c.1837G>T
CA409806471
NM_001136130.2:c.1837G>C