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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
ENSP00000398879.2:p.Phe634Leu
CA319097752
ENST00000439274.6:c.1902C>A
CA409805703
ENST00000439274.6:c.1902C>G
CA409805708
ENST00000439274.6:c.1900T>C