Canonical Allele Identifier: PA2826270650
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18100
ClinVar RCV Id: RCV000019728 RCV000084569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191231.1:p.Thr677Ile
CA127803
NM_001204302.2:c.2030C>T