Canonical Allele Identifier: PA2825818509
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98242
ClinVar RCV Id: RCV000084578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Lys668Asn
CA225514
NM_001136130.2:c.2004G>C
CA409805504
NM_001136130.2:c.2004G>T