Canonical Allele Identifier: PA2826270363
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18099
ClinVar RCV Id: RCV000019727 RCV000084562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Glu675Lys
CA127802
NM_001204301.2:c.2023G>A