Canonical Allele Identifier: PA356970
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 222971
ClinVar RCV Id: RCV000208553 RCV000522652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ile24Asn
CA356968
NM_002524.5:c.71T>A