Canonical Allele Identifier: PA916071804
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Arg68Gln
CA296059
NM_176795.5:c.203G>A