Allele Registry

Canonical Allele Identifier: PA645485979

Gene: NRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418220

RCV000418396

RCV000422640

RCV000423898

RCV000424084

RCV000426122

RCV000428055

RCV000429082

RCV000431333

RCV000433349

RCV000433761

RCV000435412

RCV000435905

RCV000436539

RCV000438738

RCV000441171

RCV000443704

RCV000444188

RCV000444754

RCV000444899

RCV002524687

ClinVar Variation:

375872

375874

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gln61Leu	CA16602359 NM_002524.5:c.182_183delinsTG CA16602361 NM_002524.5:c.182A>T CA645537992 NM_002524.5:c.181_182delinsTT