Canonical Allele Identifier: PA161314
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134991
ClinVar RCV Id: RCV000121741 RCV000680367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Met168Ile
CA161312
NM_002524.5:c.504G>C
CA341738668
NM_002524.5:c.504G>T
CA341738672
NM_002524.5:c.504G>A