Canonical Allele Identifier: PA2580278784
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1714146
ClinVar RCV Id: RCV002297129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Thr144Ala
CA341739106
NM_002524.5:c.430A>G