Canonical Allele Identifier: PA916040878
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2012Val
CA043598
NM_001354896.2:c.6035A>T