ClinGen Allele Registry
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This allele is not present in the registry. To get a canonical identifier, please click on the "Get identifier" below.
Canonical Allele Identifier:
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Gene: APP
HGNC
NCBI
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
ENSP00000387483.2:p.Lys646_Met647delinsAsnLeu
ENST00000440126.7:c.[1938G>C;1939A>C]
ENST00000440126.7:c.[1938G>C;1939A>T]
ENST00000440126.7:c.[1938G>T;1939A>C]
ENST00000440126.7:c.[1938G>T;1939A>T]
ENST00000440126.7:c.1938_1939delinsTC
