Canonical Allele Identifier: PA225503
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 98235
ClinVar RCV Id: RCV000084559 RCV003430663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.His677Arg
CA225502
NM_000484.4:c.2030A>G