Allele Registry

Canonical Allele Identifier: PA2825808495

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084560

ClinVar Variation:

98236

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Asp654Asn	CA225504 NM_001136016.3:c.1960G>A