Canonical Allele Identifier: PA2827960562
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2004Val
CA043598
NM_001354897.2:c.6011A>T