Canonical Allele Identifier: PA297025
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40473
ClinVar RCV Id: RCV000158981 RCV002470724 RCV004017274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ala59Thr
CA297023
NM_002524.5:c.175G>A