Canonical Allele Identifier: PA2828047343
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2299Asn
CA16037169
NM_001354904.2:c.6896G>A