Canonical Allele Identifier: PA2579933611
Gene: APP HGNC NCBI
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Val707Leu
CA409805599
NM_000484.4:c.2119G>T
CA409805600
NM_000484.4:c.2119G>C