Allele Registry

Canonical Allele Identifier: PA2825818938

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019714

RCV000020308

RCV000084575

RCV002496421

RCV003993747

ClinVar Variation:

18088

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Val607Ile	CA127791 NM_001136131.2:c.1819G>A