Canonical Allele Identifier: PA2741818272
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2684330
ClinVar RCV Id: RCV003482826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Val669Met
CA409806473
NM_000484.4:c.2005G>A