Canonical Allele Identifier: PA2826270381
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98240
ClinVar RCV Id: RCV000084574 RCV003509495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Ile698Thr
CA225511
NM_001204301.2:c.2093T>C