Canonical Allele Identifier: PA2827981509
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2771Pro
CA16039553
NM_001354899.2:c.8311T>C