Allele Registry

Canonical Allele Identifier: PA2826270612

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Asn623Tyr	CA409806566 NM_001204302.2:c.1867A>T