Canonical Allele Identifier: PA2826270648
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98237
ClinVar RCV Id: RCV000084567 RCV001141463
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Ala676Val
CA225505
NM_001204302.2:c.2027C>T