Canonical Allele Identifier: PA2828037343
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1007Glu
CA16028782
NM_001354904.2:c.3021T>A
CA16028783
NM_001354904.2:c.3021T>G