Canonical Allele Identifier: PA2828023155
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala1417Thr
CA16032477
NM_001354906.2:c.4249G>A