Canonical Allele Identifier: PA2741898223
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2762882
ClinVar RCV Id: RCV003540380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Phe141Leu
CA341739125
NM_002524.5:c.423C>A
CA341739127
NM_002524.5:c.423C>G
CA341739139
NM_002524.5:c.421T>C