Canonical Allele Identifier: PA658828816
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 561699
ClinVar RCV Id: RCV000681060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Glu49Asp
CA341741703
NM_002524.5:c.147A>T
CA341741704
NM_002524.5:c.147A>C