Canonical Allele Identifier: PA127798
Gene: APP HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Glu665Asp
CA127797
NM_000484.4:c.1995G>C
CA409806514
NM_000484.4:c.1995G>T