Canonical Allele Identifier: PA106121
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13900
ClinVar RCV Id: RCV000014914 RCV000032847 RCV000114744 RCV000114745 RCV000037574 RCV000424455 RCV000424721 RCV000148032 RCV000432961 RCV000420832 RCV000424960 RCV000441317 RCV000439264 RCV000419710 RCV000431883 RCV000413804 RCV000422078 RCV000422278 RCV000430407 RCV000430593 RCV000435687 RCV000438052 RCV000440367 RCV000445249 RCV003992155
ClinVar Variation Id: 375873
ClinVar RCV Id: RCV000425830
ClinVar Variation Id: 376220
ClinVar RCV Id: RCV000426087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gln61Arg
CA123618
NM_002524.5:c.182A>G
CA16602360
NM_002524.5:c.182_183delinsGG
CA16602673
NM_002524.5:c.181_182delinsAG
CA913184910
NM_002524.5:c.182_183delinsGT