Canonical Allele Identifier: PA2827981090
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2642Lys
CA16038729
NM_001354899.2:c.7925G>A