Allele Registry

Canonical Allele Identifier: PA645485966

Gene: NRAS HGNC NCBI

ClinVar RCV:

RCV000427189

ClinVar Variation:

375875

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gln61Glu	CA16602362 NM_002524.5:c.181C>G