Canonical Allele Identifier: PA2828028482
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2214Thr
CA16037620
NM_001354906.2:c.6640T>A