Canonical Allele Identifier: PA2825817952
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18098
ClinVar RCV Id: RCV000019725 RCV000020307 RCV000019726 RCV000084563
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Glu562Gly
CA127801
NM_001136129.3:c.1685A>G