Canonical Allele Identifier: PA215486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val2630Ile
CA014160
NM_001127510.3:c.7888G>A