Allele Registry

Canonical Allele Identifier: PA106185

Gene: NRAS HGNC NCBI

ClinVar Allele:

48246

ClinVar RCV:

RCV000032848

RCV000208568

ClinVar Variation:

39647

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Pro34Leu	CA130423 NM_002524.5:c.101C>T