Canonical Allele Identifier: PA2827981110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2698335
ClinVar RCV Id: RCV003536165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2648Pro
CA16038762
NM_001354899.2:c.7942A>C