Canonical Allele Identifier: PA2825818488
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18096
ClinVar RCV Id: RCV000019723 RCV000084573
ClinVar Variation Id: 1457308
ClinVar RCV Id: RCV001947096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129602.1:p.Ile660Val
CA127799
NM_001136130.2:c.1978A>G
CA2573157339
NM_001136130.2:c.1977_1978delinsTG