Canonical Allele Identifier: PA127805
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18101
ClinVar RCV Id: RCV000019729 RCV000084564 RCV000687111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Asp563Asn
CA127804
NM_001136129.3:c.1687G>A