Canonical Allele Identifier: PA658660215
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1913Val
CA16033891
NM_001127510.3:c.5737A>G