Canonical Allele Identifier: PA106185
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 39647
ClinVar RCV Id: RCV000032848 RCV000208568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Pro34Leu
CA130423
NM_002524.5:c.101C>T