Canonical Allele Identifier: PA658804036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537610
ClinVar RCV Id: RCV003538550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr46Pro
CA054190
NM_001127511.3:c.136A>C