Canonical Allele Identifier: PA2825644390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2496Ala
CA048361
NM_001127511.3:c.7486A>G