Allele Registry

Canonical Allele Identifier: PA645485944

Gene: NRAS HGNC NCBI

ClinVar RCV:

RCV000420759

ClinVar Variation:

375877

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly13Ala	CA16602364 NM_002524.5:c.38G>C