Canonical Allele Identifier: PA913200344
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1993Arg
CA16034419
NM_001127510.3:c.5978C>G