Canonical Allele Identifier: PA2828028574
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482240
ClinVar Variation Id: 642835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2231Ser
CA048379
NM_001354906.2:c.6692C>G
CA16037721
NM_001354906.2:c.6691A>T