Allele Registry

Canonical Allele Identifier: PA658674771

Gene: CDC42 HGNC NCBI

ClinVar Allele:

480736

ClinVar RCV:

RCV000577866

RCV000611080

RCV001291425

ClinVar Variation:

487652

HGVS (amino-acid)	Matching Registered Transcripts
NP_001782.1:p.Ser83Pro	CA338906853 NM_001791.4:c.247T>C