Canonical Allele Identifier: PA2828046886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2230Ser
CA16036727
NM_001354904.2:c.6688A>T
CA16036729
NM_001354904.2:c.6689C>G