Allele Registry

Canonical Allele Identifier: PA2580118028

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Asn660Ser	CA409806564 NM_000484.4:c.1979A>G