Allele Registry

Canonical Allele Identifier: PA2825818857

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Ala563Val	CA258118 NM_001136131.2:c.1688C>T