Canonical Allele Identifier: PA2828960858
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98242
ClinVar RCV Id: RCV000084578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Lys668Asn
CA225514
NM_001385253.1:c.2004G>C
CA409805504
NM_001385253.1:c.2004G>T