Allele Registry

Canonical Allele Identifier: PA645485937

Gene: NRAS HGNC NCBI

ClinVar RCV:

RCV000436341

ClinVar Variation:

376221

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly13Ser	CA16602674 NM_002524.5:c.37G>A