Canonical Allele Identifier: PA2828048812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2497Ala
CA16038426
NM_001354904.2:c.7489A>G