Allele Registry

Canonical Allele Identifier: PA2825818909

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Thr604Ala	CA127814 NM_001136131.2:c.1810A>G