Allele Registry

Canonical Allele Identifier: PA2830509001

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Val640Met	CA127800 NM_201414.3:c.1918G>A