Allele Registry

Canonical Allele Identifier: PA2828960769

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Asn604Ser	CA409806564 NM_001385253.1:c.1811A>G