Canonical Allele Identifier: PA2828036403
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser884Asn
CA348296
NM_001354904.2:c.2651G>A