Canonical Allele Identifier: PA2827980767
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2545Val
CA013990
NM_001354899.2:c.7633A>G