Canonical Allele Identifier: PA2827994177
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1079Gly
CA035284
NM_001354901.2:c.3236A>G