Canonical Allele Identifier: PA2827980474
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val2455Ala
CA16037539
NM_001354899.2:c.7364T>C