ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA127811
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001129488.1:p.Asp670Asn
NM_001136016.3:c.2008G>A