Canonical Allele Identifier: PA915998606
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 651614
ClinVar RCV Id: RCV000807015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Asp107Ala
CA341739665
NM_002524.5:c.320A>C