Canonical Allele Identifier: PA2827980404
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758666
ClinVar RCV Id: RCV002380462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2436Thr
CA16037427
NM_001354899.2:c.7306T>A