Canonical Allele Identifier: PA2828034836
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser661Gly
CA031761
NM_001354904.2:c.1981A>G