Canonical Allele Identifier: PA645476008
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 372848
ClinVar RCV Id: RCV000414468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034891.1:p.Val42Ile
CA16042336
NM_001039802.2:c.124G>A