Canonical Allele Identifier: PA193955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1286Val
CA008754
NM_001127511.3:c.3856A>G