Canonical Allele Identifier: PA2828044610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1868Val
CA043598
NM_001354904.2:c.5603A>T