Canonical Allele Identifier: PA2828025667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp1932Glu
CA010908
NM_001354903.2:c.5796C>G
CA16034682
NM_001354903.2:c.5796C>A