Allele Registry

Canonical Allele Identifier: PA2828960843

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Val659Met	CA127800 NM_001385253.1:c.1975G>A