Canonical Allele Identifier: PA177520
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 164809
ClinVar RCV Id: RCV000151575 RCV001823120 RCV001850066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Arg123Lys
CA177518
NM_002524.5:c.368G>A