Allele Registry

Canonical Allele Identifier: PA2828960767

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001939973

ClinVar Variation:

1409975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Asn604Tyr	CA409806566 NM_001385253.1:c.1810A>T