Canonical Allele Identifier: PA2828001298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly881Ser
CA033918
NM_001354902.2:c.2641G>A