Canonical Allele Identifier: PA2827942179
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser881Phe
CA348575
NM_001354895.2:c.2642C>T