Canonical Allele Identifier: PA2827998727
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2456Val
CA013792
NM_001354901.2:c.7366A>G