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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129603.1:p.Phe580Leu
CA319097752
NM_001136131.2:c.1740C>A
CA409805703
NM_001136131.2:c.1740C>G
CA409805708
NM_001136131.2:c.1738T>C