ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579933553
Gene: APP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.1324350774
Score
1.2667663085
Score
1.1649310036
Score
1.2944638671
Score
1.5721858814
Score
1.1744430197
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000475.1:p.Phe690Ser
CA409805705
NM_000484.4:c.2069T>C