Allele Registry

Canonical Allele Identifier: PA2826270348

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Ala655Val	CA258118 NM_001204301.2:c.1964C>T