Allele Registry

Canonical Allele Identifier: PA2825818475

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Thr658Ala	CA127814 NM_001136130.2:c.1972A>G