Canonical Allele Identifier: PA2828960802
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98235
ClinVar RCV Id: RCV000084559 RCV003430663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.His621Arg
CA225502
NM_001385253.1:c.1862A>G