Canonical Allele Identifier: PA297022
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40468
ClinVar RCV Id: RCV000158979 RCV000422059 RCV000422738 RCV000425805 RCV000433830 RCV000440380 RCV000435186 RCV000444830 RCV000432311 RCV000445013 RCV002291497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Cys
CA297020
NM_002524.5:c.34G>T