Canonical Allele Identifier: PA658810032
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 208668
ClinVar RCV Id: RCV000190678 RCV000601199 RCV001291422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001782.1:p.Arg66Gly
CA204641
NM_001791.4:c.196A>G