Allele Registry

Canonical Allele Identifier: PA2828960841

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Thr658Ala	CA127814 NM_001385253.1:c.1972A>G