Canonical Allele Identifier: PA2826270388
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1342870
ClinVar RCV Id: RCV001842233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Thr701Pro
CA409805542
NM_001204301.2:c.2101A>C