Allele Registry

Canonical Allele Identifier: PA2830509015

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000084578

ClinVar Variation:

98242

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Lys649Asn	CA225514 NM_201414.3:c.1947G>C CA409805504 NM_201414.3:c.1947G>T