Canonical Allele Identifier: PA2825818397
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_001129602.1:p.Val613Met
CA409806473
NM_001136130.2:c.1837G>A