Canonical Allele Identifier: PA2825818934
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18089
ClinVar RCV Id: RCV000019715 RCV000815476 RCV002054452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129603.1:p.Val607Phe
CA127792
NM_001136131.2:c.1819G>T