Canonical Allele Identifier: PA2827980774
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 960729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2547Pro
CA16038103
NM_001354899.2:c.7639T>C