Canonical Allele Identifier: PA2827980698
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2524Cys
CA16037960
NM_001354899.2:c.7570A>T