Allele Registry

Canonical Allele Identifier: PA2826270912

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Val622Met	CA127800 NM_001204303.2:c.1864G>A