Canonical Allele Identifier: PA297032
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40469
ClinVar RCV Id: RCV000158985 RCV000420637 RCV000444217 RCV000420396 RCV000423088 RCV000430635 RCV000438291 RCV000435447 RCV000440262 RCV000425150 RCV000430032 RCV001526619 RCV001781335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Arg
CA297030
NM_002524.5:c.34G>C