Canonical Allele Identifier: PA067337
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 219097
ClinVar RCV Id: RCV000203450 RCV000380895 RCV000426950 RCV000427550 RCV000418647 RCV000434113 RCV000444591 RCV000425963 RCV000433455 RCV000437165 RCV000444670 RCV001324275 RCV001813426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Ala
CA280928
NM_002524.5:c.35G>C