Canonical Allele Identifier: PA2827998757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2467Arg
CA048553
NM_001354901.2:c.7400A>G