Canonical Allele Identifier: PA2825818878
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18087
ClinVar RCV Id: RCV000019713 RCV001386879 RCV002272024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129603.1:p.Glu583Gln
CA127790
NM_001136131.2:c.1747G>C