Allele Registry

Canonical Allele Identifier: PA2826270385

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019714

RCV000020308

RCV000084575

RCV002496421

RCV003993747

ClinVar Variation:

18088

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Val699Ile	CA127791 NM_001204301.2:c.2095G>A