Allele Registry

Canonical Allele Identifier: PA2825818839

Gene: APP HGNC NCBI

ClinVar RCV:

RCV002653213

ClinVar Variation:

1937323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129603.1:p.Asn550Ser	CA409806564 NM_001136131.2:c.1649A>G