Canonical Allele Identifier: PA2827943017
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1133Glu
CA16028782
NM_001354895.2:c.3399T>A
CA16028783
NM_001354895.2:c.3399T>G