Canonical Allele Identifier: PA2827947274
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2422Ala
CA012961
NM_001354895.2:c.7264A>G