Canonical Allele Identifier: PA916040877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2011Arg
CA16034419
NM_001354896.2:c.6032C>G