Canonical Allele Identifier: PA296076
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180856
ClinVar RCV Id: RCV000463046 RCV000505776 RCV002258816 RCV002492617 RCV003390855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg169Gln
CA296075
NM_005343.4:c.506G>A