Canonical Allele Identifier: PA16040105
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly2370Val
CA046963
NM_000038.6:c.7109G>T