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
ENSP00000346129.3:p.Lys539_Met540delinsAsnLeu
ENST00000354192.7:c.[1617G>C;1618A>C]
ENST00000354192.7:c.[1617G>C;1618A>T]
ENST00000354192.7:c.[1617G>T;1618A>C]
ENST00000354192.7:c.[1617G>T;1618A>T]
ENST00000354192.7:c.1617_1618delinsTC
