Canonical Allele Identifier: PA2499232734
Gene: APP HGNC NCBI
ClinVar RCV:
RCV001727209
ClinVar Variation:
1298879
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Ile716Met
CA409805552
NM_000484.4:c.2148C>G