Canonical Allele Identifier: PA2573308949
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1406399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Arg68Trp
CA378924631
NM_176795.5:c.202C>T