ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825808506
Gene: APP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
932452
ClinVar RCV Id:
RCV001200266
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001129488.1:p.Leu664Val
CA409806217
NM_001136016.3:c.1990T>G