Canonical Allele Identifier: PA2580278776
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1723143
ClinVar RCV Id: RCV002306250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ile55Thr
CA341741663
NM_002524.5:c.164T>C