Allele Registry

Canonical Allele Identifier: PA2825808460

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Asn636Tyr	CA409806566 NM_001136016.3:c.1906A>T