Canonical Allele Identifier: PA1139706696
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 836160
ClinVar RCV Id: RCV001037216 RCV001261055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ser183Asn
CA378920937
NM_005343.4:c.548G>A