Canonical Allele Identifier: PA2825644876
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761670
ClinVar RCV Id: RCV002419243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2655Ile
CA16038747
NM_001127511.3:c.7964G>T