Canonical Allele Identifier: PA2827975593
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser982Asn
CA348296
NM_001354899.2:c.2945G>A