Canonical Allele Identifier: PA645402540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val2686Ala
CA049793
NM_001127510.3:c.8057T>C