Canonical Allele Identifier: PA2827987951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1953Val
CA043598
NM_001354900.2:c.5858A>T