Allele Registry

Canonical Allele Identifier: PA2830509011

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019714

RCV000020308

RCV000084575

RCV002496421

RCV003993747

ClinVar Variation:

18088

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Val642Ile	CA127791 NM_201414.3:c.1924G>A