Canonical Allele Identifier: PA164314
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2795Thr
CA015437
NM_001127510.3:c.8383G>A