Canonical Allele Identifier: PA2828001630
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1047Gly
CA035284
NM_001354902.2:c.3140A>G