Allele Registry

Canonical Allele Identifier: PA2825818498

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Val661Leu	CA127816 NM_001136130.2:c.1981G>C