Canonical Allele Identifier: PA2827971412
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2490Val
CA013792
NM_001354898.2:c.7468A>G