Canonical Allele Identifier: PA2827980851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2570Ser
CA16038256
NM_001354899.2:c.7708A>T
CA16038257
NM_001354899.2:c.7709C>G