Canonical Allele Identifier: PA2827986871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 653217
ClinVar RCV Id: RCV002537302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu1627Gly
CA16032280
NM_001354900.2:c.4880A>G