Canonical Allele Identifier: PA2825630399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1138Gly
CA035284
NM_001127510.3:c.3413A>G