Canonical Allele Identifier: PA297946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2626Ile
CA014137
NM_000038.6:c.7877C>T