Allele Registry

Canonical Allele Identifier: PA183540

Gene: NRAS HGNC NCBI

ClinVar Allele:

172330

ClinVar RCV:

RCV000155806

RCV000373742

RCV000654962

RCV001261093

RCV003945240

ClinVar Variation:

179025

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Pro185Ser	CA183538 NM_002524.5:c.553C>T