Allele Registry

Canonical Allele Identifier: PA2830508747

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_958816.1:p.Asn641Tyr	CA409806566 NM_201413.3:c.1921A>T