ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579986254
Gene: APP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.499731244
Score
1.2077553754
Score
1.0034061237
Score
1.0291198683
Score
1.0304083755
Score
1.0875289079
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000475.1:p.Leu688Ser
CA409806212
NM_000484.4:c.2063T>C