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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Thr701Ser
CA409805538
NM_001204301.2:c.2102C>G
CA409805540
NM_001204301.2:c.2101A>T