Canonical Allele Identifier: PA2827997015
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1935Val
CA043598
NM_001354901.2:c.5804A>T