Canonical Allele Identifier: PA658809667
Gene: RHOA HGNC NCBI

Linked Data

ClinVar Variation Id: 521191
ClinVar RCV Id: RCV000623047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001655.1:p.Tyr66His
CA352786786
NM_001664.4:c.196T>C