Allele Registry

Canonical Allele Identifier: PA356970

Gene: NRAS HGNC NCBI

ClinVar RCV:

RCV000208553

RCV000522652

ClinVar Variation:

222971

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Ile24Asn	CA356968 NM_002524.5:c.71T>A