Canonical Allele Identifier: PA2828960775
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Glu609Asp
CA127797
NM_001385253.1:c.1827G>C
CA409806514
NM_001385253.1:c.1827G>T