Allele Registry

Canonical Allele Identifier: PA2825808458

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129488.1:p.Asn636Ser	CA409806564 NM_001136016.3:c.1907A>G