Canonical Allele Identifier: PA2826270338
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Glu647Asp
CA127797
NM_001204301.2:c.1941G>C
CA409806514
NM_001204301.2:c.1941G>T