Allele Registry

Canonical Allele Identifier: PA2826270376

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Val697Met	CA127800 NM_001204301.2:c.2089G>A