Canonical Allele Identifier: PA2828018696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly871Ser
CA033918
NM_001354903.2:c.2611G>A