Allele Registry

Canonical Allele Identifier: PA2825808510

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019717

RCV000019718

RCV000020306

RCV000084561

ClinVar Variation:

18091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Ala668Gly	CA127794 NM_001136016.3:c.2003C>G