Canonical Allele Identifier: PA2828029737
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val2403Ala
CA049793
NM_001354906.2:c.7208T>C