Canonical Allele Identifier: PA2827962794
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2684Pro
CA16038751
NM_001354897.2:c.8050T>C