Canonical Allele Identifier: PA2828028325
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1345335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Phe2361Ser
CA16037417
NM_001354903.2:c.7082T>C