Canonical Allele Identifier: PA645485971
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 280409
ClinVar RCV Id: RCV000291285 RCV000426654 RCV000428903 RCV000430000 RCV000421496 RCV000432170 RCV000427746 RCV000431592 RCV000437545 RCV000439526 RCV000439765 RCV000444660 RCV000419053 RCV000419201 RCV000421291 RCV000434604 RCV000444278 RCV000420302 RCV000437312 RCV000438468 RCV003155143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gln61Pro
CA10602732
NM_002524.5:c.182A>C