Canonical Allele Identifier: PA2825642112
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1761Met
CA041612
NM_001127511.3:c.5283A>G