Allele Registry

Canonical Allele Identifier: PA2830508802

Gene: APP HGNC NCBI

ClinVar Allele:

104133

ClinVar RCV:

RCV000084577

ClinVar Variation:

98241

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Leu704Pro	CA225513 NM_201413.3:c.2111T>C