Canonical Allele Identifier: PA2826270645
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_001191231.1:p.Gly672Ser
CA9987055
NM_001204302.2:c.2014G>A