Canonical Allele Identifier: PA2580278786
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2074072
ClinVar RCV Id: RCV002976028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gln150His
CA341739002
NM_002524.5:c.450G>T
CA341739003
NM_002524.5:c.450G>C