Canonical Allele Identifier: PA658659718
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1159Arg
CA16028963
NM_001127510.3:c.3476C>G