Canonical Allele Identifier: PA2828009435
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser1884Asn
CA043925
NM_001354905.2:c.5651G>A