Allele Registry

Canonical Allele Identifier: PA2573169967

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Asn660Tyr	CA409806566 NM_000484.4:c.1978A>T