Canonical Allele Identifier: PA204642
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 208668
ClinVar RCV Id: RCV000190678 RCV000601199 RCV001291422
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034891.1:p.Arg66Gly
CA204641
NM_001039802.2:c.196A>G