Allele Registry

Canonical Allele Identifier: PA2826270868

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Asn567Tyr	CA409806566 NM_001204303.2:c.1699A>T