Canonical Allele Identifier: PA2827974695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala712Thr
CA16026193
NM_001354899.2:c.2134G>A