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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191232.1:p.Phe597Leu
CA319097752
NM_001204303.2:c.1791C>A
CA409805703
NM_001204303.2:c.1791C>G
CA409805708
NM_001204303.2:c.1789T>C