ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826270633
Gene: APP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001200266
ClinVar Variation:
932452
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191231.1:p.Leu651Val
CA409806217
NM_001204302.2:c.1951T>G