Canonical Allele Identifier: PA2826270386
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18105
ClinVar RCV Id: RCV000518713 RCV000019733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191230.1:p.Val699Leu
CA127816
NM_001204301.2:c.2095G>C