Canonical Allele Identifier: PA113559
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18099
ClinVar RCV Id: RCV000019727 RCV000084562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Glu693Lys
CA127802
NM_000484.4:c.2077G>A