Canonical Allele Identifier: PA2827998417
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2363Ala
CA012961
NM_001354901.2:c.7087A>G