Allele Registry

Canonical Allele Identifier: PA106165

Gene: NRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

28940

ClinVar RCV:

RCV000014915

RCV000022690

RCV000144962

RCV000157672

RCV000421229

RCV000421906

RCV000422699

RCV000430350

RCV000431020

RCV000431528

RCV000433031

RCV000440357

RCV000440593

RCV000442419

RCV001293767

ClinVar Variation:

13901

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly13Asp	CA123620 NM_002524.5:c.38G>A