Canonical Allele Identifier: PA2828048834
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2500Ala
CA049327
NM_001354904.2:c.7498A>G