Canonical Allele Identifier: PA2828960797
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 37145
ClinVar RCV Id: RCV000030774 RCV000084558 RCV002513276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372182.1:p.Ala617Thr
CA130092
NM_001385253.1:c.1849G>A