Canonical Allele Identifier: PA113527
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98236
ClinVar RCV Id: RCV000084560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Asp678Asn
CA225504
NM_000484.4:c.2032G>A