Allele Registry

Canonical Allele Identifier: PA106155

Gene: NRAS HGNC NCBI

Linked Data

ClinVar RCV:

RCV000014913

RCV000114743

RCV000419545

RCV000419583

RCV000424942

RCV000426328

RCV000427817

RCV000428963

RCV000434327

RCV000437450

RCV000438070

RCV000444449

RCV001781267

ClinVar Variation:

13899

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly13Arg	CA151261 NM_002524.5:c.37G>C