Allele Registry

Canonical Allele Identifier: PA2828960854

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019733

RCV000518713

ClinVar Variation:

18105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Val661Leu	CA127816 NM_001385253.1:c.1981G>C