Canonical Allele Identifier: PA2827998722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2455Ala
CA048361
NM_001354901.2:c.7363A>G