Canonical Allele Identifier: PA2828018388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala827Thr
CA007787
NM_001354903.2:c.2479G>A