Allele Registry

Canonical Allele Identifier: PA278805

Gene: CDC42 HGNC NCBI

ClinVar Allele:

215784

ClinVar RCV:

RCV000203307

RCV000489915

RCV001266021

RCV001291421

ClinVar Variation:

218950

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034891.1:p.Tyr64Cys	CA278804 NM_001039802.2:c.191A>G