Canonical Allele Identifier: PA2825643964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2361Pro
CA16036870
NM_001127511.3:c.7081A>C