Canonical Allele Identifier: PA2827989658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2473Ala
CA048361
NM_001354900.2:c.7417A>G