Canonical Allele Identifier: PA2825818479
Gene: APP HGNC NCBI
ClinVar RCV:
RCV000084571
ClinVar Variation:
98238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Val659Ala
CA225507
NM_001136130.2:c.1976T>C