Allele Registry

Canonical Allele Identifier: PA2830508787

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Thr695Ala	CA127814 NM_201413.3:c.2083A>G