Canonical Allele Identifier: PA916071803
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 120223
ClinVar RCV Id: RCV000106320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Glu63_Asp69dup
CA267613
NM_176795.5:c.187_207dup