Canonical Allele Identifier: PA2828029113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala2475Thr
CA16038108
NM_001354903.2:c.7423G>A