Canonical Allele Identifier: PA2828011948
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1345335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Phe2371Ser
CA16037417
NM_001354902.2:c.7112T>C