Canonical Allele Identifier: PA2827979308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2107Val
CA044550
NM_001354899.2:c.6319A>G