Canonical Allele Identifier: PA296056
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180848
ClinVar RCV Id: RCV000157914 RCV000418565 RCV000418712 RCV000427265 RCV000429433 RCV000434580 RCV000436822 RCV000442670 RCV000444507 RCV000419846 RCV000421468 RCV000424767 RCV000426169 RCV000428389 RCV000432148 RCV000437080 RCV000439230 RCV000444587 RCV000590121 RCV001255688 RCV001849323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly13Val
CA296055
NM_005343.4:c.38G>T