Canonical Allele Identifier: PA2827987847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His1924Pro
CA043314
NM_001354900.2:c.5771A>C