Canonical Allele Identifier: PA2579986156
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Asn698Lys
CA409805653
NM_000484.4:c.2094C>G
CA409805654
NM_000484.4:c.2094C>A