Canonical Allele Identifier: PA106145
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 39648
ClinVar RCV Id: RCV000032849 RCV000144963 RCV000158980 RCV000439064 RCV000440963 RCV000424239 RCV000427949 RCV000434517 RCV000417702 RCV000417869 RCV000430706 RCV000436228 RCV001781333 RCV001813214 RCV001852659 RCV003221788 RCV003415756 RCV004018703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Asp
CA130425
NM_002524.5:c.35G>A