Canonical Allele Identifier: PA916071747
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 690298
ClinVar RCV Id: RCV000860022
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Thr58_Ala59delinsValLeuAspVal
CA915948742
NM_176795.5:c.172_177delinsGTCCTGGATGTT