Allele Registry

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Canonical Allele Identifier: PA2826270659

Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18096

ClinVar RCV Id: RCV000019723 RCV000084573

ClinVar Variation Id: 1457308

ClinVar RCV Id: RCV001947096

JSON-LD

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Ile679Val	CA127799 NM_001204302.2:c.2035A>G CA2573157339 NM_001204302.2:c.2034_2035delinsTG