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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001129601.1:p.Lys539_Met540delinsAsnLeu
NM_001136129.3:c.[1617G>C;1618A>C]

NM_001136129.3:c.[1617G>C;1618A>T]

NM_001136129.3:c.[1617G>T;1618A>C]

NM_001136129.3:c.[1617G>T;1618A>T]

NM_001136129.3:c.1617_1618delinsTC