Canonical Allele Identifier: PA2825644420
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470098
ClinVar RCV Id: RCV003537085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile2510Val
CA16037809
NM_001127511.3:c.7528A>G