Canonical Allele Identifier: PA2827996911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His1906Pro
CA043314
NM_001354901.2:c.5717A>C