Allele Registry

Canonical Allele Identifier: PA297032

Gene: NRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

48939

ClinVar RCV:

RCV000158985

RCV000420396

RCV000420637

RCV000423088

RCV000425150

RCV000430032

RCV000430635

RCV000435447

RCV000438291

RCV000440262

RCV000444217

RCV001526619

RCV001781335

ClinVar Variation:

40469

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly12Arg	CA297030 NM_002524.5:c.34G>C