Canonical Allele Identifier: PA2827990401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2697Thr
CA336116
NM_001354900.2:c.8090T>C