Allele Registry

Canonical Allele Identifier: PA113590

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019730

RCV000084568

RCV002513124

ClinVar Variation:

18102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Thr714Ala	CA127814 NM_000484.4:c.2140A>G