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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000346129.3:p.Leu589Phe
ENST00000354192.7:c.1767G>C

ENST00000354192.7:c.1767G>T