Canonical Allele Identifier: PA2829600814
Gene: HRAS HGNC NCBI
ClinVar Allele:
677975
ClinVar RCV:
RCV000860022
ClinVar Variation:
690298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr58_Ala59delinsValLeuAspVal
CA915948742
NM_005343.4:c.172_177delinsGTCCTGGATGTT