Canonical Allele Identifier: PA2828016205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr461Met
CA005437
NM_001354903.2:c.1382C>T