Allele Registry

Canonical Allele Identifier: PA2825817997

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019714

RCV000020308

RCV000084575

RCV002496421

RCV003993747

ClinVar Variation:

18088

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Val586Ile	CA127791 NM_001136129.3:c.1756G>A