Allele Registry

Canonical Allele Identifier: PA127810

Gene: APP HGNC NCBI

ClinVar Allele:

33140

ClinVar RCV:

RCV000019729

RCV000084564

RCV000687111

ClinVar Variation:

18101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191231.1:p.Asp657Asn	CA127804 NM_001204302.2:c.1969G>A