ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826270869
Gene: APP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002653213
ClinVar Variation:
1937323
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191232.1:p.Asn567Ser
CA409806564
NM_001204303.2:c.1700A>G