Canonical Allele Identifier: PA645402044
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2384Ile
CA047103
NM_001127510.3:c.7150T>A