Canonical Allele Identifier: PA2579933759
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.His685Gln
CA409806252
NM_000484.4:c.2055T>G
CA409806253
NM_000484.4:c.2055T>A