Canonical Allele Identifier: PA129949
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12613
ClinVar RCV Id: RCV000013447 RCV000029211 RCV000032851 RCV000212495 RCV000418395 RCV000424087 RCV000427213 RCV000428012 RCV000419553 RCV000149829 RCV000436505 RCV000439243 RCV000429404 RCV000434677 RCV000438707 RCV000440052 RCV000443678 RCV000443826 RCV000444512 RCV000422023 RCV000424380 RCV000431815 RCV000438902 RCV000421701 RCV000426992 RCV000429096 RCV000431602 RCV000762849 RCV000436802 RCV000437868 RCV000445233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Cys
CA129948
NM_005343.4:c.34G>T