Canonical Allele Identifier: PA2827947851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2733518
ClinVar RCV Id: RCV003535123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly2597Leu
CA2697546408
NM_001354895.2:c.7789_7790delinsTT