Canonical Allele Identifier: PA2827998194
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2297Ser
CA16036727
NM_001354901.2:c.6889A>T
CA16036729
NM_001354901.2:c.6890C>G