ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825817942
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_001129601.1:p.Leu557Val
CA409806217
NM_001136129.3:c.1669T>G