Allele Registry

Canonical Allele Identifier: PA2825817940

Gene: APP HGNC NCBI

ClinVar RCV:

RCV003397222

ClinVar Variation:

2628367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129601.1:p.Lys556Asn	CA409806220 NM_001136129.3:c.1668A>T CA409806222 NM_001136129.3:c.1668A>C