Canonical Allele Identifier: PA2579933719
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Asp678Glu
CA409806345
NM_000484.4:c.2034C>A
CA409806347
NM_000484.4:c.2034C>G