Canonical Allele Identifier: PA645486020
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 424299
ClinVar RCV Id: RCV000480705 RCV001100797 RCV001066150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ile84Val
CA1020748
NM_002524.5:c.250A>G