Allele Registry

Canonical Allele Identifier: PA2830508960

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Asn585Ser	CA409806564 NM_201414.3:c.1754A>G