Canonical Allele Identifier: PA658678982
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 450081
ClinVar RCV Id: RCV000521930 RCV002527601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ala155Val
CA1020690
NM_002524.5:c.464C>T