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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001129488.1:p.Lys646_Met647delinsAsnLeu
NM_001136016.3:c.[1938G>C;1939A>C]

NM_001136016.3:c.[1938G>C;1939A>T]

NM_001136016.3:c.[1938G>T;1939A>C]

NM_001136016.3:c.[1938G>T;1939A>T]

NM_001136016.3:c.1938_1939delinsTC