Canonical Allele Identifier: PA2828039855
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met1287Val
CA009368
NM_001354904.2:c.3859A>G