Allele Registry

Canonical Allele Identifier: PA180755

Gene: NRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000158978

RCV000212761

RCV000421327

RCV000421993

RCV000427184

RCV000430288

RCV000431995

RCV000433097

RCV000439216

RCV000442594

RCV000445150

RCV001066799

RCV001813397

RCV003998247

ClinVar Variation:

177778

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly12Ser	CA180753 NM_002524.5:c.34G>A