Canonical Allele Identifier: PA156752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2541Val
CA013946
NM_000038.6:c.7621A>G