Canonical Allele Identifier: PA2828043433
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1716Thr
CA042221
NM_001354904.2:c.5146T>A