Canonical Allele Identifier: PA278805
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 218950
ClinVar RCV Id: RCV000203307 RCV000489915 RCV001266021 RCV001291421
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Amino-acid Alleles

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