Canonical Allele Identifier: PA2832441599
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Met671Ile
CA409806432
NM_000484.4:c.2013G>T
CA409806434
NM_000484.4:c.2013G>C
CA409806436
NM_000484.4:c.2013G>A