Canonical Allele Identifier: PA2828028607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2396Thr
CA16037620
NM_001354903.2:c.7186T>A