Canonical Allele Identifier: PA2827966468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1001Thr
CA16028070
NM_001354898.2:c.3002A>C