Canonical Allele Identifier: PA2825817997
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18088
ClinVar RCV Id: RCV000019714 RCV000020308 RCV000084575 RCV003993747 RCV002496421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Val586Ile
CA127791
NM_001136129.3:c.1756G>A