Allele Registry

Canonical Allele Identifier: PA2828960821

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019713

RCV001386879

RCV002272024

ClinVar Variation:

18087

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Glu637Gln	CA127790 NM_001385253.1:c.1909G>C