Canonical Allele Identifier: PA106165
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13901
ClinVar RCV Id: RCV000014915 RCV000022690 RCV000144962 RCV000157672 RCV000431528 RCV000430350 RCV000433031 RCV000421906 RCV000440593 RCV000440357 RCV000421229 RCV000422699 RCV000431020 RCV000442419 RCV001293767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly13Asp
CA123620
NM_002524.5:c.38G>A