Canonical Allele Identifier: PA2830508782
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 638317
ClinVar RCV Id: RCV000790931 RCV000790930 RCV001869244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Gly690Ser
CA9987055
NM_201413.3:c.2068G>A