Canonical Allele Identifier: PA106197
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13902
ClinVar RCV Id: RCV000014916 RCV000211835 RCV000208537 RCV000463185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Thr50Ile
CA257019
NM_002524.5:c.149C>T