Canonical Allele Identifier: PA658659316
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly637Arg
CA16025491
NM_001127510.3:c.1909G>A
CA16025492
NM_001127510.3:c.1909G>C