Canonical Allele Identifier: PA645399548
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1140Arg
CA16028829
NM_001127510.3:c.3419C>G