Allele Registry

Canonical Allele Identifier: PA2825818505

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001842233

ClinVar Variation:

1342870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129602.1:p.Thr663Pro	CA409805542 NM_001136130.2:c.1987A>C