Canonical Allele Identifier: PA2827978873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1966Val
CA043598
NM_001354899.2:c.5897A>T