Canonical Allele Identifier: PA658816352
Gene: RRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 527794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006261.1:p.Val190Leu
CA9578960
NM_006270.5:c.568G>C