Canonical Allele Identifier: PA127798
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Glu665Asp
CA127797
NM_000484.4:c.1995G>C
CA409806514
NM_000484.4:c.1995G>T