Canonical Allele Identifier: PA113599
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Thr714Ile
CA127803
NM_000484.4:c.2141C>T