Allele Registry

Canonical Allele Identifier: PA2830509013

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001842233

ClinVar Variation:

1342870

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Thr644Pro	CA409805542 NM_201414.3:c.1930A>C