Canonical Allele Identifier: PA2579933593
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Phe691Leu
CA409805695
NM_000484.4:c.2073T>A
CA409805696
NM_000484.4:c.2073T>G
CA409805701
NM_000484.4:c.2071T>C