Allele Registry

Canonical Allele Identifier: PA2826270909

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Thr621Ala	CA127814 NM_001204303.2:c.1861A>G