Allele Registry

Canonical Allele Identifier: PA127808

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019729

RCV000084564

RCV000687111

ClinVar Variation:

18101

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Asp619Asn	CA127804 NM_201414.3:c.1855G>A