Canonical Allele Identifier: PA2826270665
Gene: APP HGNC NCBI
ClinVar Allele:
104133
ClinVar RCV:
RCV000084577
ClinVar Variation:
98241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Leu686Pro
CA225513
NM_001204302.2:c.2057T>C