Allele Registry

Canonical Allele Identifier: PA2825808485

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019734

ClinVar Variation:

18106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Ala649Val	CA258118 NM_001136016.3:c.1946C>T