Canonical Allele Identifier: PA658660257
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His1965Arg
CA16034228
NM_001127510.3:c.5894A>G