Allele Registry

Canonical Allele Identifier: PA2825818443

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019717

RCV000019718

RCV000020306

RCV000084561

ClinVar Variation:

18091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Ala636Gly	CA127794 NM_001136130.2:c.1907C>G