Canonical Allele Identifier: PA2827968631
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1648Gly
CA16032310
NM_001354898.2:c.4943A>G