Canonical Allele Identifier: PA2827954065
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val1133Met
CA035105
NM_001354896.2:c.3397G>A