Canonical Allele Identifier: PA2828016156
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu447Val
CA16024895
NM_001354903.2:c.1339T>G