Allele Registry

Canonical Allele Identifier: PA2826270375

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Thr696Ala	CA127814 NM_001204301.2:c.2086A>G