Canonical Allele Identifier: PA2826270657
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2498894
ClinVar RCV Id: RCV003223103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Ile679Phe
CA409805555
NM_001204302.2:c.2035A>T