Canonical Allele Identifier: PA2828047983
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile2389Val
CA013792
NM_001354904.2:c.7165A>G