Canonical Allele Identifier: PA2827966862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1113Gly
CA035284
NM_001354898.2:c.3338A>G