Canonical Allele Identifier: PA2828029026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val2460Ile
CA16038011
NM_001354903.2:c.7378G>A