Canonical Allele Identifier: PA658681817
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser112Pro
CA034347
NM_001127511.3:c.334T>C