Allele Registry

Canonical Allele Identifier: PA2830509014

Gene: APP HGNC NCBI

ClinVar Allele:

104133

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Leu648Pro	CA225513 NM_201414.3:c.1943T>C