Canonical Allele Identifier: PA2830508765
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98236
ClinVar RCV Id: RCV000084560
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Asp659Asn
CA225504
NM_201413.3:c.1975G>A