Canonical Allele Identifier: PA2828033401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr436Met
CA005437
NM_001354904.2:c.1307C>T