Canonical Allele Identifier: PA130093
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 37145
ClinVar RCV Id: RCV000030774 RCV000084558 RCV002513276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Ala673Thr
CA130092
NM_000484.4:c.2017G>A