Canonical Allele Identifier: PA156793
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2286Val
CA012589
NM_001127510.3:c.6857C>T