Allele Registry

Canonical Allele Identifier: PA2828960798

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Ala617Val	CA258118 NM_001385253.1:c.1850C>T