Canonical Allele Identifier: PA2825642283
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1818Arg
CA042181
NM_001127511.3:c.5452G>A
CA16033377
NM_001127511.3:c.5452G>C