Canonical Allele Identifier: PA2828021615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr1165Ile
CA16030848
NM_001354906.2:c.3494C>T