ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826270654
Gene: APP
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191231.1:p.Val678Met
CA127800
NM_001204302.2:c.2032G>A