Allele Registry

Canonical Allele Identifier: PA2826270389

Gene: APP HGNC NCBI

ClinVar Allele:

104133

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Leu705Pro	CA225513 NM_001204301.2:c.2114T>C