Canonical Allele Identifier: PA2827990017
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2585Ile
CA014137
NM_001354900.2:c.7754C>T