Canonical Allele Identifier: PA2828025079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp1711Val
CA043598
NM_001354906.2:c.5132A>T