Canonical Allele Identifier: PA2828020745
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1029Ala
CA008783
NM_001354906.2:c.3086G>C