Allele Registry

Canonical Allele Identifier: PA2826270371

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084567

RCV001141463

ClinVar Variation:

98237

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Ala695Val	CA225505 NM_001204301.2:c.2084C>T