Canonical Allele Identifier: PA2827948151
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val2686Ala
CA049793
NM_001354895.2:c.8057T>C