Canonical Allele Identifier: PA2827981389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2728Val
CA014501
NM_001354899.2:c.8182A>G