Canonical Allele Identifier: PA2827985113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1097Gly
CA035284
NM_001354900.2:c.3290A>G