Canonical Allele Identifier: PA2827980578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482240
ClinVar Variation Id: 642835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2486Ser
CA048379
NM_001354899.2:c.7457C>G
CA16037721
NM_001354899.2:c.7456A>T