Allele Registry

Canonical Allele Identifier: PA2830508987

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019713

RCV001386879

RCV002272024

ClinVar Variation:

18087

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Glu618Gln	CA127790 NM_201414.3:c.1852G>C