Canonical Allele Identifier: PA2825691854
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 462149
ClinVar RCV Id: RCV000546898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Glu62_Arg68dup
CA658656102
NM_001130442.3:c.186_206dup