Canonical Allele Identifier: PA164312
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2777Thr
CA015437
NM_001127511.3:c.8329G>A