Canonical Allele Identifier: PA2827966871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1115Arg
CA16028829
NM_001354898.2:c.3344C>G