Canonical Allele Identifier: PA2827980123
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2351Ser
CA047031
NM_001354899.2:c.7052C>G
CA16036872
NM_001354899.2:c.7051A>T