Canonical Allele Identifier: PA2830508786
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18094
ClinVar RCV Id: RCV000547582 RCV000826088 RCV002272025 RCV000019721 RCV000084566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Ala694Thr
CA090906
NM_201413.3:c.2080G>A