Canonical Allele Identifier: PA1139709596
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 981572
ClinVar RCV Id: RCV001261091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Thr148Ile
CA341739039
NM_002524.5:c.443C>T