Allele Registry

Canonical Allele Identifier: PA2826270335

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Asn642Ser	CA409806564 NM_001204301.2:c.1925A>G