Allele Registry

Canonical Allele Identifier: PA2826270391

Gene: APP HGNC NCBI

ClinVar RCV:

RCV001141462

ClinVar Variation:

897923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Lys707Asn	CA409805496 NM_001204301.2:c.2121G>T CA409805497 NM_001204301.2:c.2121G>C