Canonical Allele Identifier: PA2830508967
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2684330
ClinVar RCV Id: RCV003482826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958817.1:p.Val594Met
CA409806473
NM_201414.3:c.1780G>A