Canonical Allele Identifier: PA106126
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 73058
ClinVar RCV Id: RCV000114746 RCV000144964 RCV000425440 RCV000426976 RCV000428264 RCV000428499 RCV000436588 RCV000418269 RCV000418907 RCV000431313 RCV000434388 RCV000435041 RCV000441559 RCV000436806 RCV000423656 RCV000443974 RCV000444882 RCV000423012 RCV000433274 RCV000441348 RCV000444538 RCV000626456 RCV000696329 RCV000662267 RCV001092890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gln61Lys
CA151263
NM_002524.5:c.181C>A
CA645537989
NM_002524.5:c.181_183delinsAAG
CA645537993
NM_002524.5:c.180_181delinsTA
CA645537994
NM_002524.5:c.180_181delinsCA
CA891841769
NM_002524.5:c.180_181delinsGA