Allele Registry

Canonical Allele Identifier: PA106170

Gene: NRAS HGNC NCBI

ClinVar Allele:

28942

ClinVar RCV:

RCV000014917

RCV000158982

RCV000208552

RCV001382056

RCV003415702

ClinVar Variation:

13903

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly60Glu	CA257021 NM_002524.5:c.179G>A