Canonical Allele Identifier: PA2741898217
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2639009
ClinVar RCV Id: RCV003406685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Lys88Asn
CA341741374
NM_002524.5:c.264G>T
CA341741376
NM_002524.5:c.264G>C