Allele Registry

Canonical Allele Identifier: PA2826270374

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019728

RCV000084569

ClinVar Variation:

18100

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Thr696Ile	CA127803 NM_001204301.2:c.2087C>T