Canonical Allele Identifier: PA113626
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_000475.1:p.Val717Ile
CA127791
NM_000484.4:c.2149G>A