Allele Registry

Canonical Allele Identifier: PA2825818439

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Lys631Asn	CA409806220 NM_001136130.2:c.1893A>T CA409806222 NM_001136130.2:c.1893A>C