Canonical Allele Identifier: PA2828053814
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr466Ala
CA029787
NM_001354905.2:c.1396A>G