Allele Registry

Canonical Allele Identifier: PA645485940

Gene: NRAS HGNC NCBI

ClinVar RCV:

RCV000445167

ClinVar Variation:

40471

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gly13Cys	CA16602248 NM_002524.5:c.37G>T CA2844645830 NM_002524.5:c.36_37delinsGT