Canonical Allele Identifier: PA261527
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40470
ClinVar RCV Id: RCV000037576 RCV000158986 RCV000421072 RCV000423890 RCV000432178 RCV000419124 RCV000429393 RCV000438750 RCV000438967 RCV000439421 RCV001377735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Val
CA261525
NM_002524.5:c.35G>T