Canonical Allele Identifier: PA645486028
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291976
ClinVar RCV Id: RCV002356400 RCV000262996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Thr127Arg
CA1020717
NM_002524.5:c.380C>G