Canonical Allele Identifier: PA913201990
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 450370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_426359.1:p.Arg68Gln
CA338906652
NM_044472.3:c.203G>A