Canonical Allele Identifier: PA2825808495
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98236
ClinVar RCV Id: RCV000084560
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Asp654Asn
CA225504
NM_001136016.3:c.1960G>A