Canonical Allele Identifier: PA297905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2404Ala
CA012961
NM_001127511.3:c.7210A>G