Canonical Allele Identifier: PA2828033271
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile418Thr
CA005403
NM_001354904.2:c.1253T>C