Canonical Allele Identifier: PA2826270377
Gene: APP HGNC NCBI
ClinVar RCV:
RCV000084571
ClinVar Variation:
98238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Val697Ala
CA225507
NM_001204301.2:c.2090T>C