Canonical Allele Identifier: PA2827985200
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1119Ala
CA035507
NM_001354900.2:c.3355A>G