Allele Registry

Canonical Allele Identifier: PA2579933630

Gene: APP HGNC NCBI

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Met706Ile	CA409805601 NM_000484.4:c.2118G>T CA409805602 NM_000484.4:c.2118G>C CA409805603 NM_000484.4:c.2118G>A