Canonical Allele Identifier: PA2825640489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1236Val
CA036589
NM_001127511.3:c.3706A>G