Canonical Allele Identifier: PA2829600814
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 690298
ClinVar RCV Id: RCV000860022

Amino-acid Alleles

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