Canonical Allele Identifier: PA2827989354
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2381Ala
CA012961
NM_001354900.2:c.7141A>G