ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826270384
Gene: APP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
18090
ClinVar RCV Id:
RCV000019716
RCV000084576
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191230.1:p.Val699Gly
CA127793
NM_001204301.2:c.2096T>G