Canonical Allele Identifier: PA2827964229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser274Thr
CA051068
NM_001354898.2:c.820T>A