Allele Registry

Canonical Allele Identifier: PA2828960855

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001842233

ClinVar Variation:

1342870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Thr663Pro	CA409805542 NM_001385253.1:c.1987A>C