Canonical Allele Identifier: PA2828028952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile2290Val
CA013990
NM_001354906.2:c.6868A>G