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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001129488.1:p.Phe667Leu
NM_001136016.3:c.1999T>C

NM_001136016.3:c.2001T>A

NM_001136016.3:c.2001T>G