Canonical Allele Identifier: PA2828027499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2073Ser
CA16036727
NM_001354906.2:c.6217A>T
CA16036729
NM_001354906.2:c.6218C>G