Canonical Allele Identifier: PA2828028379
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2198Ser
CA16037526
NM_001354906.2:c.6592A>T
CA16037528
NM_001354906.2:c.6593C>G