Canonical Allele Identifier: PA2825387567
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 450370
ClinVar RCV Id: RCV000519757 RCV001332038 RCV001291423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034891.1:p.Arg68Gln
CA338906652
NM_001039802.2:c.203G>A