Allele Registry

Canonical Allele Identifier: PA2580118033

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002642603

ClinVar Variation:

1936601

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Thr663Met	CA9987104 NM_000484.4:c.1988C>T